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Mutations on the Protein: P40692 From Positions: 680 To 718

6
4
1
1


Swiss-Prot Polymorphism: VAR_004466
p.ALA681THR
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_012931
p.ARG687TRP
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_012932
p.GLN689ARG
N/A
N/A
N/A


dbSNP Polymorphism: rs2020873
p.HIS718TYR
N/A
N/A


Swiss-Prot Polymorphism: VAR_012933
p.VAL716MET
N/A
N/A
N/A


OMIM Disease: 120436.0022
p.ALA681THR
N/A
N/A
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2






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