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Mutations on the Protein: P51798 From Positions: 483 To 523

2
2
0
0











Swiss-Prot Disease: VAR_064642
p.GLY521ARG
N/A
N/A
Osteopetrosis, autosomal recessive 4 (OPTB4)


Swiss-Prot Disease: VAR_021003
p.LEU490PHE
N/A
N/A
Osteopetrosis, autosomal dominant 2 (OPTA2)






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