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Mutations on the Protein: NP_001447 From Positions: 1188 To 1320

3
0
0
3




OMIM Disease: 300017.0012
p.ALA1188THR
N/A
N/A
MELNICK-NEEDLES SYNDROME


OMIM Disease: 300017.0028
p.PRO1291LEU
N/A
N/A
FG SYNDROME 2


OMIM Disease: 300017.0013
p.SER1199LEU
N/A
N/A
MELNICK-NEEDLES SYNDROME






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