Allele Registry

Canonical Allele Identifier: PA915957810

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012961

RCV002472928

ClinVar Variation:

12179

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Arg409Cys	CA3732711 NM_000500.9:c.1225C>T