Canonical Allele Identifier: PA2580233492
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 2441174
ClinVar RCV Id: RCV003147003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Tyr304Asp
CA413449025
NM_001399.5:c.910T>G