Allele Registry

Canonical Allele Identifier: PA2580124538

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV003060031

ClinVar Variation:

2136375

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Arg427Pro	CA363511963 NM_000500.9:c.1280G>C