Allele Registry

Canonical Allele Identifier: PA341182

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012937

RCV000711368

RCV003407321

ClinVar Variation:

12152

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Arg357Trp	CA341181 NM_000500.9:c.1069C>T