Canonical Allele Identifier: PA095687
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 418171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Gly255Asp
CA16621473
NM_001399.5:c.764G>A