Allele Registry

Canonical Allele Identifier: PA2828286106

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012954

RCV003234903

ClinVar Variation:

12172

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Glu246Asp	CA3732657 NM_001368144.1:c.738G>C CA363511265 NM_001368144.1:c.738G>T