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Mutations on the Protein: NP_001161089 From Positions: 494 To 526

2
0
0
2



OMIM Disease: 120436.0033
p.LEU524HIS
N/A
N/A
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2


OMIM Disease: 120436.0012
p.LYS520ALA
N/A
N/A
RECLASSIFIED - VARIANT OF UNKNOWN SIGNIFICANCE






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