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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRAS
(V160M)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
KRAS
(T58I)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic