Allele Registry

Canonical Allele Identifier: PA2828286119

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012961

RCV002472928

ClinVar Variation:

12179

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Arg274Cys	CA3732711 NM_001368144.1:c.820C>T