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Mutations on the Protein: P35499 From Positions: 1561 To 1652

4
2
0
2



Swiss-Prot Disease: VAR_001575
p.MET1592VAL
N/A
N/A
Periodic paralysis normokalemic (NKPP)


Swiss-Prot Disease: VAR_001574
p.VAL1589MET
N/A
N/A
Paramyotonia congenita of von Eulenburg (PMC)


OMIM Disease: 603967.0002
p.MET1592VAL
N/A
N/A
HYPERKALEMIC PERIODIC PARALYSIS||PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS, INCLUDED


OMIM Disease: 603967.0009
p.VAL1589MET
N/A
N/A
MYOTONIA, POTASSIUM-AGGRAVATED||PARAMYOTONIA CONGENITA, INCLUDED






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