Allele Registry

Canonical Allele Identifier: PA915957819

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012957

RCV001851813

RCV003390673

ClinVar Variation:

12175

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Arg427His	CA136895676 NM_000500.9:c.1280G>A