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Mutations on the Protein: NP_001129601 From Positions: 543 To 575

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OMIM Disease: 104760.0005
p.ALA561GLY
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT||ALZHEIMER DISEASE, FAMILIAL, 1, INCLUDED


OMIM Disease: 104760.0016
p.ASN563ASP
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT


OMIM Disease: 104760.0001
p.GLU562GLN
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT


OMIM Disease: 104760.0013
p.GLU562GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1||CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT, INCLUDED


OMIM Disease: 104760.0014
p.GLU562LYS
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT


OMIM Disease: 104760.0019
p.LEU574VAL
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT






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