Canonical Allele Identifier: PA658676764
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 451037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Thr333Arg
CA413449743
NM_001399.5:c.998C>G