Canonical Allele Identifier: PA2825273969
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 996827
ClinVar RCV Id: RCV001291628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Gly207Glu
CA413448363
NM_001005609.2:c.620G>A