ClinGen Allele Registry
Centralized resource standardizing allele identifiers across multiple genomic databases.
What it does
Ensures that variants mapped across disparate population databases represent the precise same genomic alteration.
STRC usage
Not yet tested on E1659A.
Connections
- STRC Variant c.4976A>C — Misha [see-also]
- STRC Gene [about]
[part-of]Tools index