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Mutations on the Protein: O60890 From Positions: 40 To 80

2
1
0
1











Swiss-Prot Polymorphism: VAR_013638
p.ALA45THR
N/A
N/A
N/A


OMIM Disease: 300127.0003
p.GLN62TER
N/A
N/A
MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE||FACIAL APPEARANCE






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