Allele Registry

Canonical Allele Identifier: PA645381492

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000490344

RCV001357310

RCV003155127

ClinVar Variation:

225335

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Ala392Thr	CA3732662 NM_000500.9:c.1174G>A