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1 protein found in SwissVar (0 variants)

with gene/protein name P35499

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)
P35499 SCN4A_HUMAN paramyotonia congenita of von eulenburg
P35499 SCN4A_HUMAN periodic paralysis hypokalemic 2
P35499 SCN4A_HUMAN periodic paralysis hyperkalemic
P35499 SCN4A_HUMAN periodic paralysis normokalemic
P35499 SCN4A_HUMAN myotonia scn4a-related
P35499 SCN4A_HUMAN myasthenic syndrome, congenital, 16
P35499 SCN4A_HUMAN an autosomal recessive neuromuscular disorder characterized by severe fetal hypokinesia, neonatal hypotonia and congenital myopathy of variable severity