Allele Registry

Canonical Allele Identifier: PA341184

Gene: CYP21A2 HGNC NCBI

ClinVar Allele:

27192

ClinVar RCV:

RCV000012938

RCV000711390

ClinVar Variation:

12153

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Pro31Leu	CA341183 NM_000500.9:c.92C>T