Canonical Allele Identifier: PA133758
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44212
ClinVar RCV Id: RCV000037190 RCV002513473
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Glu294Val
CA133757
NM_001399.5:c.881A>T