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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAMT
(Q148fs)
Duplication
(frameshift variant)
Cerebral creatine deficiency syndrome
+1 more
GPathogenic
GAMT
(T136M)
Single nucleotide variant
(missense variant)
Deficiency of guanidinoacetate methyltransferase
GPathogenic
GAMT
(D135N)
Single nucleotide variant
(missense variant)
Deficiency of guanidinoacetate methyltransferase
GPathogenic
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