Canonical Allele Identifier: PA2825274566
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 418174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Ala377Thr
CA16621477
NM_001005612.3:c.1129G>A