Canonical Allele Identifier: PA645484048
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 381658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Gly165Ala
CA16609205
NM_001399.5:c.494G>C