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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OAT
Deletion
(splice donor variant +1 more)
Ornithine aminotransferase deficiency
GPathogenic
OAT
(P138L)
Single nucleotide variant
(missense variant +2 more)
Ornithine aminotransferase deficiency
GUncertain significance