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Mutations on the Protein: P48544 From Positions: 147 To 168

4
3
0
1



Swiss-Prot Disease: VAR_065930
p.GLY151ARG
N/A
N/A
Familial hyperaldosteronism 3 (FH3)


Swiss-Prot Disease: VAR_067090
p.GLY151GLU
N/A
N/A
Familial hyperaldosteronism 3 (FH3)


Swiss-Prot Disease: VAR_065931
p.THR158ALA
N/A
N/A
Familial hyperaldosteronism 3 (FH3)


OMIM Disease: 600734.0002
p.THR158ALA
N/A
N/A
HYPERALDOSTERONISM, FAMILIAL, TYPE III






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