Canonical Allele Identifier: PA658676726
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 458657
ClinVar RCV Id: RCV000559389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Ser160Asn
CA413447991
NM_001399.5:c.479G>A