Allele Registry

Canonical Allele Identifier: PA2828285956

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000711388

RCV003317352

ClinVar Variation:

585757

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355072.1:p.Leu173Val	CA136894756 NM_001368143.1:c.517T>G