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Mutations on the Protein: P01116 From Positions: 19 To 28

2
2
0
0














































































Swiss-Prot Disease: VAR_064851
p.GLN22ARG
N/A
N/A
Noonan syndrome 3 (NS3)


Swiss-Prot Disease: VAR_064850
p.GLN22GLU
N/A
N/A
Cardiofaciocutaneous syndrome 2 (CFC2)






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