Canonical Allele Identifier: PA095720
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44211
ClinVar RCV Id: RCV000037189 RCV000256153 RCV003398602
ClinVar Variation Id: 1918319
ClinVar RCV Id: RCV002601900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Gly291Arg
CA261508
NM_001399.5:c.871G>A
CA413448923
NM_001399.5:c.871G>C