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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


1 records found for search term Fdx1l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8628195CV83339single nucleotide variantNM_001031734.3(FDX1L):c.26C>A (p.Ala9Asp)Malignant melanoma [RCV000063419]not provided191031598010315980Humanname