SWISSVAR
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1 protein found in SwissVar (0 variants)

with gene/protein name P03905

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)
P03905 NU4M_HUMAN leber hereditary optic neuropathy
P03905 NU4M_HUMAN leber hereditary optic neuropathy with dystonia
P03905 NU4M_HUMAN mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome