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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTPN11
(N308D +1 more)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic
PTPN11
(R498W +2 more)
Single nucleotide variant
(missense variant)
Metachondromatosis
+10 more
GPathogenic