Allele Registry

Canonical Allele Identifier: PA2825669187

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002481158

ClinVar Variation:

1809584

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Val276Gly	CA363507470 NM_001128590.3:c.827T>G