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1 protein found in SwissVar (3 variants)

with gene/protein name P19367

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)
P19367 HXK1_HUMAN hexokinase deficiency p.Leu529Ser

P19367 HXK1_HUMAN neuropathy, hereditary motor and sensory, russe type
P19367 HXK1_HUMAN retinitis pigmentosa 79 p.Glu847Lys