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Pathways
Variants search result for All species
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1 records found for search term B3galt5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8628610CV83754single nucleotide variantNM_006057.2(B3GALT5):c.905C>T (p.Ser302Phe)Malignant melanoma [RCV000063835]not provided213966146439661464Humanname