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Pathways
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2 records found for search term Sept12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8627823CV82967single nucleotide variantNM_144605.4(SEPT12):c.334G>A (p.Asp112Asn)Malignant melanoma [RCV000063047]not provided1647858474785847Humanname
8635821CV91044single nucleotide variantNM_144605.4(SEPT12):c.1022C>T (p.Pro341Leu)Malignant melanoma [RCV000071142]not provided1647778524777852Humanname