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Mutations on the Protein: NP_001129488 From Positions: 671 To 709

10
0
0
10



OMIM Disease: 104760.0009
p.ALA689THR
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0011
p.ILE692VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0019
p.LEU681VAL
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT


OMIM Disease: 104760.0017
p.THR690ALA
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0015
p.THR690ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0004
p.VAL693GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0002
p.VAL693ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0021
p.VAL693LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0012
p.VAL691MET
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0003
p.VAL693PHE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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