Canonical Allele Identifier: PA2825273928
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Arg156Cys
CA255655
NM_001005609.2:c.466C>T