Canonical Allele Identifier: PA2825274023
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44209
ClinVar RCV Id: RCV000037187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Trp274Cys
CA261505
NM_001005609.2:c.822G>T
CA413448817
NM_001005609.2:c.822G>C