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Mutations on the Protein: Q96S42 From Positions: 174 To 191

2
1
0
1


Swiss-Prot Disease: VAR_015111
p.ARG183GLN
N/A
N/A
Heterotaxy, visceral, 5, autosomal (HTX5)


OMIM Disease: 601265.0001
p.ARG183GLN
N/A
N/A
HETEROTAXY, VISCERAL, 5, AUTOSOMAL






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