Canonical Allele Identifier: PA096021
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11031
ClinVar RCV Id: RCV000011778 RCV000763629
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Tyr61His
CA255649
NM_001399.5:c.181T>C