Canonical Allele Identifier: PA2825274456
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44211
ClinVar Variation Id: 1918319
ClinVar RCV Id: RCV002601900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Gly288Arg
CA261508
NM_001005612.3:c.862G>A
CA413448923
NM_001005612.3:c.862G>C