Allele Registry

Canonical Allele Identifier: PA2828286010

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000991861

RCV002249597

ClinVar Variation:

804725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355072.1:p.Gly290Ser	CA3732715 NM_001368143.1:c.868G>A