Canonical Allele Identifier: PA2825274052
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Glu294Val
CA133757
NM_001005609.2:c.881A>T