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Mutations on the Protein: NP_001170782 From Positions: 0 To 101

2
0
1
1


dbSNP Polymorphism: rs1333342
p.THR2ILE
N/A
N/A
N/A


OMIM Disease: 607009.0008
p.ARG51TER
N/A
N/A
HYPOMAGNESEMIA WITH SECONDARY HYPOCALCEMIA


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