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Mutations on the Protein: NP_001121135 From Positions: 153 To 192

2
0
0
2



OMIM Disease: 137350.0001
p.ASP172ASN
N/A
N/A
AMYLOIDOSIS, FAMILIAL, FINNISH TYPE||AMYLOIDOSIS, MERETOJA TYPE


OMIM Disease: 137350.0002
p.ASP172TYR
N/A
N/A
AMYLOIDOSIS, FAMILIAL, FINNISH TYPE






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