Canonical Allele Identifier: PA2825274127
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 265112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Arg355Trp
CA10588798
NM_001005609.2:c.1063C>T