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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAMT, LOC130062945
Deletion
(splice donor variant)
Deficiency of guanidinoacetate methyltransferase
GPathogenic
GAMT, LOC130062945
(G61R)
Single nucleotide variant
(missense variant)
Cerebral creatine deficiency syndrome
+1 more
GLikely pathogenic