Allele Registry

Canonical Allele Identifier: PA2825669165

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001269963

RCV002250459

RCV002298442

ClinVar Variation:

12173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Val208Glu	CA358442 NM_001128590.3:c.623T>A