Canonical Allele Identifier: PA645484210
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 426389
ClinVar RCV Id: RCV000489664 RCV003479140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Tyr311His
CA413449247
NM_001399.5:c.931T>C