Canonical Allele Identifier: PA095397
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11040
ClinVar RCV Id: RCV000011787 RCV000255050
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Ala349Thr
CA255657
NM_001399.5:c.1045G>A