Canonical Allele Identifier: PA2825274119
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Ala347Thr
CA255657
NM_001005609.2:c.1039G>A