Allele Registry

Canonical Allele Identifier: PA2828285951

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012940

RCV000711386

ClinVar Variation:

12156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355072.1:p.Gly157Ser	CA256231 NM_001368143.1:c.469G>A