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Mutations on the Protein: NP_001177397 From Positions: 91 To 103

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OMIM Disease: 600837.0001
p.ARG93TRP
N/A
N/A
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3||CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, INCLUDED;;||PHEOCHROMOCYTOMA,






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