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Mutations on the Protein: Q99707 From Positions: 886 To 949

3
1
1
1









dbSNP Polymorphism: rs1805087
p.ASP919GLY
N/A
N/A
N/A


Swiss-Prot Disease: VAR_004330
p.HIS920ASP
N/A
N/A
Homocystinuria-megaloblastic anemia, cblG complementation type (HMAG)


OMIM Disease: 156570.0003
p.HIS920ASP
N/A
N/A
HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblG COMPLEMENTATION TYPE






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