Canonical Allele Identifier: PA2825274289
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Tyr61His
CA255649
NM_001005612.3:c.181T>C