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Mutations on the Protein: NP_000892 From Positions: 492 To 541

2
0
1
1


dbSNP Polymorphism: rs5526
p.ARG537GLN
N/A
N/A
N/A


OMIM Disease: 600983.0003
p.ARG537TER
N/A
N/A
PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT






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