Allele Registry

Canonical Allele Identifier: PA129646

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000024069

RCV000029655

RCV000055819

RCV000252481

RCV001529036

ClinVar Variation:

12154

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Ser269Thr	CA129645 NM_000500.9:c.806G>C