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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAF1
Single nucleotide variant
(intron variant +1 more)
Noonan syndrome 5
+2 more
GConflicting classifications of pathogenicity
RAF1
(S257L +3 more)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome
GPathogenic
RAF1
(T10M)
Single nucleotide variant
(missense variant +2 more)
RASopathy
+2 more
GUncertain significance
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