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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NALCN
(M547V +1 more)
Single nucleotide variant
(missense variant)
Congenital contractures of the limbs and face, hypotonia, and developmental delay
GLikely pathogenic
NALCN
(I322T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GPathogenic/Likely pathogenic