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Mutations on the Protein: NP_005594 From Positions: 626 To 688

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0
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1



OMIM Disease: 602397.0006
p.ILE661THR
N/A
N/A
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1||CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1, INCLUDED






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