Allele Registry

Canonical Allele Identifier: PA344930

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000055817

RCV000245772

RCV000711377

ClinVar Variation:

65608

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Arg103Lys	CA344929 NM_000500.9:c.308G>A