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Mutations on the Protein: P55895 From Positions: 26 To 53

3
1
0
2


Swiss-Prot Disease: VAR_008895
p.CYS41TRP
N/A
N/A
Omenn syndrome (OS)


OMIM Disease: 179616.0008
p.ARG39GLY
N/A
N/A
SEVERE COMBINED IMMUNODEFICIENCY, B CELL-NEGATIVE||OMENN SYNDROME, INCLUDED


OMIM Disease: 179616.0003
p.CYS41TRP
N/A
N/A
OMENN SYNDROME






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