Canonical Allele Identifier: PA645484153
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 372608
ClinVar RCV Id: RCV000413515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Gly257Arg
CA16043329
NM_001399.5:c.769G>C
CA413448690
NM_001399.5:c.769G>A