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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NALCN
Deletion
(splice acceptor variant)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
GPathogenic
NALCN
Deletion
(nonsense)
Hypotonia, infantile, with psychomotor retardation and characteristic facies 1
GPathogenic/Likely pathogenic
NALCN
(R152*)
Single nucleotide variant
(nonsense)
Congenital contractures of the limbs and face, hypotonia, and developmental delay
+1 more
GPathogenic
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