Canonical Allele Identifier: PA2499232967
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1264327
ClinVar RCV Id: RCV001667853
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Gly425Val
CA363511936
NM_000500.9:c.1274G>T