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Mutations on the Protein: P55895 From Positions: 211 To 237

2
0
0
2


OMIM Disease: 179616.0002
p.ARG229GLN
N/A
N/A
SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE||OMENN SYNDROME, INCLUDED


OMIM Disease: 179616.0007
p.TRP215ILE
N/A
N/A
SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE






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