Canonical Allele Identifier: PA2828286123
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_001355073.1:p.Gly290Val
CA363511936
NM_001368144.1:c.869G>T