Allele Registry

Canonical Allele Identifier: PA2828286045

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001269963

RCV002250459

RCV002298442

ClinVar Variation:

12173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Val103Glu	CA358442 NM_001368144.1:c.308T>A