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Mutations on the Protein: P15169 From Positions: 160 To 183

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Swiss-Prot Disease: VAR_042415
p.GLY178ASP
N/A
N/A
Carboxypeptidase N deficiency (CPND)


dbSNP Polymorphism: rs61751507
p.GLY178VAL
N/A
N/A
N/A


OMIM Disease: 603103.0002
p.GLY178ASP
N/A
N/A
CARBOXYPEPTIDASE N DEFICIENCY






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