Allele Registry

Canonical Allele Identifier: PA256237

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012966

ClinVar Variation:

18452

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Lys121Gln	CA256236 NM_000500.9:c.361A>C