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Mutations on the Protein: NP_000375 From Positions: 2053 To 2282

2
0
0
2


OMIM Disease: 107730.0006
p.ARG2058TER
N/A
N/A
HYPOBETALIPOPROTEINEMIA, FAMILIAL, ASSOCIATED WITH APOB46


OMIM Disease: 107730.0013
p.GLN2252TER
N/A
N/A
HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC






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