Canonical Allele Identifier: PA2825274529
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Ala344Thr
CA255657
NM_001005612.3:c.1030G>A