Allele Registry

Canonical Allele Identifier: PA2825669184

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012940

RCV000711386

ClinVar Variation:

12156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Gly262Ser	CA256231 NM_001128590.3:c.784G>A