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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A19
Single nucleotide variant
(intron variant)
Neutral 1 amino acid transport defect
+2 more
GUncertain significance
SLC6A19
(V324I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance