Allele Registry

Canonical Allele Identifier: PA2825669226

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012954

RCV003234903

ClinVar Variation:

12172

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Glu351Asp	CA3732657 NM_001128590.3:c.1053G>C CA363511265 NM_001128590.3:c.1053G>T