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1 protein found in SwissVar (0 variants)

with gene/protein name P51788

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)
P51788 CLCN2_HUMAN epilepsy, idiopathic generalized 11
P51788 CLCN2_HUMAN juvenile absence epilepsy 2
P51788 CLCN2_HUMAN juvenile myoclonic epilepsy 8
P51788 CLCN2_HUMAN leukoencephalopathy with ataxia
P51788 CLCN2_HUMAN hyperaldosteronism, familial, 2