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Mutations on the Protein: P01116 From Positions: 66 To 76

2
1
0
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Swiss-Prot Disease: VAR_069784
p.TYR71HIS
N/A
N/A
Cardiofaciocutaneous syndrome 2 (CFC2)


OMIM Disease: 190070.0021
p.TYR71HIS
N/A
N/A
CARDIOFACIOCUTANEOUS SYNDROME 2






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