Canonical Allele Identifier: PA095418
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 228255
ClinVar RCV Id: RCV000809933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Ala356Val
CA10577181
NM_001399.5:c.1067C>T