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Mutations on the Protein: P50440 From Positions: 190 To 212

2
1
0
1




Swiss-Prot Disease: VAR_069816
p.TYR203SER
N/A
N/A
Cerebral creatine deficiency syndrome 3 (CCDS3)


OMIM Disease: 602360.0005
p.TYR203SER
N/A
N/A
CEREBRAL CREATINE DEFICIENCY SYNDROME 3






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