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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NTRK2
(I71V)
Single nucleotide variant
(missense variant)
Obesity, hyperphagia, and developmental delay
+1 more
GConflicting classifications of pathogenicity
NTRK2
(T161I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NTRK2
(A187E +1 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
NTRK2
(G307S +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NTRK2
(K656T +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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