Allele Registry

Canonical Allele Identifier: PA915957813

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000991861

RCV002249597

ClinVar Variation:

804725

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Gly425Ser	CA3732715 NM_000500.9:c.1273G>A