Canonical Allele Identifier: PA095944
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11048
ClinVar RCV Id: RCV000011795 RCV001205829
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Thr338Met
CA121314
NM_001399.5:c.1013C>T