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Pathways
Variants search result for All species
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1 records found for search term H1foo
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8625502CV80625single nucleotide variantNM_153833.1(H1FOO):c.414G>A (p.Arg138=)Malignant melanoma [RCV000060702]not provided3129549036129549036Humanname