A resource for standardized human genetic variant nomenclature, helping researchers and clinicians accurately name and reference genetic changes.
Standardize genetic variant names easily
Varnomen by HGVS is a specialized resource dedicated to the standardized naming of human genetic variants. If you work with genetic data in research or clinical settings, this site guides you through the correct way to describe and reference genetic changes according to international standards.
You can use Varnomen to ensure your genetic variant descriptions are clear and consistent, which is essential for sharing findings and collaborating with others in the genetics field. Whether you're a seasoned researcher, a clinician, or a student learning about genetics, this tool helps you avoid confusion and communicate effectively.
The site stands out by offering authoritative guidance on variant nomenclature, making it easier for you to stay up-to-date and maintain accuracy in your genetic reports and publications.
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