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1 protein found in SwissVar (0 variants)

with gene/protein name P26358

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)
P26358 DNMT1_HUMAN neuropathy, hereditary sensory, 1e
P26358 DNMT1_HUMAN cerebellar ataxia, deafness, and narcolepsy, autosomal dominant