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Mutations on the Protein: NP_001447 From Positions: 528 To 660

2
0
0
2





OMIM Disease: 300017.0006
p.LEU656PHE
N/A
N/A
HETEROTOPIA, PERIVENTRICULAR NODULAR, X-LINKED DOMINANT


OMIM Disease: 300017.0030
p.PRO637GLN
N/A
N/A
CARDIAC VALVULAR DYSPLASIA, X-LINKED






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