Allele Registry

Canonical Allele Identifier: PA915971579

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000055817

RCV000245772

RCV000711377

ClinVar Variation:

65608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Arg73Lys	CA344929 NM_001128590.3:c.218G>A