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1 protein found in SwissVar (1 variants)

with gene/protein name P42658

Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.

Accession Entry name Disease Variants 3D mapping
(variant position)
P42658 DPP6_HUMAN familial paroxysmal ventricular fibrillation 2
P42658 DPP6_HUMAN mental retardation, autosomal dominant 33 p.Met385Leu