Canonical Allele Identifier: PA261483
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44188
ClinVar RCV Id: RCV000037164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Leu55Gln
CA261482
NM_001399.5:c.164T>A