Canonical Allele Identifier: PA645484161
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 372359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg276Leu
CA16043276
NM_001399.5:c.827G>T