Allele Registry

Canonical Allele Identifier: PA891849535

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000711388

RCV003317352

ClinVar Variation:

585757

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Leu308Val	CA136894756 NM_000500.9:c.922T>G