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Mutations on the Protein: P56539 From Positions: 76 To 83

4
2
0
2


Swiss-Prot Disease: VAR_043696
p.LEU79ARG
N/A
N/A
Sudden infant death syndrome (SIDS)


Swiss-Prot Disease: VAR_043695
p.THR78MET
N/A
N/A
Sudden infant death syndrome (SIDS)


OMIM Disease: 601253.0021
p.LEU79ARG
N/A
N/A
LONG QT SYNDROME 9


OMIM Disease: 601253.0018
p.THR78MET
N/A
N/A
LONG QT SYNDROME 9||LONG QT SYNDROME 2/9, DIGENIC, INCLUDED






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