Allele Registry

Canonical Allele Identifier: PA2825669246

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV003060031

ClinVar Variation:

2136375

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Arg397Pro	CA363511963 NM_001128590.3:c.1190G>C