Allele Registry

Canonical Allele Identifier: PA2828286128

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000984580

ClinVar Variation:

800602

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Gly296Ser	CA363511998 NM_001368144.1:c.886G>A