Canonical Allele Identifier: PA2825669243
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_001122062.3:p.Gly395Val
CA363511936
NM_001128590.3:c.1184G>T