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1 protein found in SwissVar (0 variants)

with gene/protein name P68133

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)
P68133 ACTS_HUMAN nemaline myopathy 3
P68133 ACTS_HUMAN myopathy, actin, congenital, with excess of thin myofilaments
P68133 ACTS_HUMAN myopathy, congenital, with fiber-type disproportion
P68133 ACTS_HUMAN myopathy, scapulohumeroperoneal