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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAMK2B
(P139L)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 54
+3 more
GPathogenic/Likely pathogenic
CAMK2B
(A111P)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 54
GUncertain significance
CAMK2B
(E110K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
CAMK2B
(T8N)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 54
GUncertain significance
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