Allele Registry

Canonical Allele Identifier: PA2825669248

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000984580

ClinVar Variation:

800602

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Gly401Ser	CA363511998 NM_001128590.3:c.1201G>A