Allele Registry

Canonical Allele Identifier: PA358443

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001269963

RCV002250459

RCV002298442

ClinVar Variation:

12173

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Val238Glu	CA358442 NM_000500.9:c.713T>A