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Mutations on the Protein: P22309 From Positions: 53 To 80

2
0
1
1


dbSNP Disease: rs4148323
p.GLY71ARG
N/A
Transient familial neonatal hyperbilirubinemia (HBLRTFN)


OMIM Disease: 191740.0016
p.GLY71ARG
N/A
N/A
GILBERT SYNDROME||HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL, INCLUDED;;||BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE T






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