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Mutations on the Protein: P02489 From Positions: 17 To 26

3
1
0
2



Swiss-Prot Disease: VAR_046892
p.ARG21LEU
N/A
N/A
Cataract 9, multiple types (CTRCT9)


OMIM Disease: 123580.0010
p.ARG21GLN
N/A
N/A
CATARACT 9, NUCLEAR LAMELLAR


OMIM Disease: 123580.0009
p.ARG21TRP
N/A
N/A
CATARACT 9, MULTIPLE TYPES, WITH MICROCORNEA






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