Canonical Allele Identifier: PA2825274107
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Thr336Met
CA121314
NM_001005609.2:c.1007C>T