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Mutations on the Protein: P01116 From Positions: 151 To 161

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0
0
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OMIM Disease: 190070.0010,190070.0015
p.ASP153VAL
N/A
N/A
NOONAN SYNDROME 3


OMIM Disease: 190070.0018
p.PHE156LEU
N/A
N/A
CARDIOFACIOCUTANEOUS SYNDROME 2


OMIM Disease: 190070.0014
p.VAL152GLY
N/A
N/A
NOONAN SYNDROME 3






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