Canonical Allele Identifier: PA2825273927
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Arg156His
CA261114
NM_001005609.2:c.467G>A