Canonical Allele Identifier: PA133746
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44189
ClinVar RCV Id: RCV000037165 RCV000622517
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Leu58del
CA133745
NM_001399.5:c.173_175del
CA413447222
NM_001399.5:c.173T>A