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Mutations on the Protein: Q13635 From Positions: 362 To 434

3
2
0
1



Swiss-Prot Disease: VAR_032952
p.ALA393THR
N/A
N/A
Holoprosencephaly 7 (HPE7)


Swiss-Prot Disease: VAR_007844
p.PHE376SER
N/A
N/A
Basal cell nevus syndrome (BCNS)


OMIM Disease: 601309.0011
p.ALA393THR
N/A
N/A
HOLOPROSENCEPHALY 7






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