Canonical Allele Identifier: PA2825274363
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44197
ClinVar Variation Id: 44198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Asn185_Pro196del
CA261494
NM_001005612.3:c.546_581del
CA261496
NM_001005612.3:c.553_588del