Canonical Allele Identifier: PA2825274345
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Arg156Cys
CA255655
NM_001005612.3:c.466C>T