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Mutations on the Protein: Q13635 From Positions: 1013 To 1085

3
2
0
1



Swiss-Prot Disease: VAR_010979
p.GLY1069ARG
N/A
N/A
Basal cell nevus syndrome (BCNS)


Swiss-Prot Disease: VAR_032958
p.THR1052MET
N/A
N/A
Holoprosencephaly 7 (HPE7)


OMIM Disease: 601309.0014
p.THR1052MET
N/A
N/A
HOLOPROSENCEPHALY 7






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