Allele Registry

Canonical Allele Identifier: PA2580124481

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002481158

ClinVar Variation:

1809584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Val306Gly	CA363507470 NM_000500.9:c.917T>G