Allele Registry

Canonical Allele Identifier: PA2825669186

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002211046

RCV002281650

ClinVar Variation:

1675317

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Val275Met	CA3732569 NM_001128590.3:c.823G>A