Canonical Allele Identifier: PA095537
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg69Leu
CA255650
NM_001399.5:c.206G>T