Allele Registry

Canonical Allele Identifier: PA121920

Gene: CYP21A2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000012934

RCV000012935

RCV000012936

RCV000055820

RCV000210728

RCV000711385

RCV001804725

RCV003407320

ClinVar Variation:

12151

65610

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Val282Leu	CA121919 NM_000500.9:c.844G>T CA344933 NM_000500.9:c.844G>C