Allele Registry

Canonical Allele Identifier: PA915957820

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000984580

ClinVar Variation:

800602

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Gly431Ser	CA363511998 NM_000500.9:c.1291G>A