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Mutations on the Protein: P51798 From Positions: 644 To 684

2
2
0
0








Swiss-Prot Disease: VAR_021006
p.GLY677VAL
N/A
N/A
Osteopetrosis, autosomal dominant 2 (OPTA2)


Swiss-Prot Disease: VAR_064645
p.LEU651PRO
N/A
N/A
Osteopetrosis, autosomal recessive 4 (OPTB4)






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