Allele Registry

Canonical Allele Identifier: PA256232

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012940

RCV000711386

ClinVar Variation:

12156

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Gly292Ser	CA256231 NM_000500.9:c.874G>A