Allele Registry

Canonical Allele Identifier: PA2825669242

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000991861

RCV002249597

ClinVar Variation:

804725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Gly395Ser	CA3732715 NM_001128590.3:c.1183G>A