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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GOT2
(G376D +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 82
GUncertain significance
GOT2
(P78L)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 82
+1 more
GUncertain significance