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Mutations on the Protein: P01116 From Positions: 28 To 38

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Swiss-Prot Disease: VAR_064854
p.ILE36MET
N/A
N/A
Noonan syndrome 3 (NS3)


Swiss-Prot Disease: VAR_026110
p.PRO34ARG
N/A
N/A
Cardiofaciocutaneous syndrome 2 (CFC2)


Swiss-Prot Disease: VAR_064853
p.PRO34GLN
N/A
N/A
Noonan syndrome 3 (NS3)


Swiss-Prot Disease: VAR_064852
p.PRO34LEU
N/A
N/A
Noonan syndrome 3 (NS3)


OMIM Disease: 190070.0013
p.PRO34ARG
N/A
N/A
CARDIOFACIOCUTANEOUS SYNDROME 2






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