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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NALCN
(E1226G +2 more)
Single nucleotide variant
(missense variant)
Congenital contractures of the limbs and face, hypotonia, and developmental delay
GUncertain significance
NALCN
(G1087C +2 more)
Single nucleotide variant
(missense variant)
Congenital contractures of the limbs and face, hypotonia, and developmental delay
GBenign
NALCN
(K1051E +2 more)
Single nucleotide variant
(missense variant)
Congenital contractures of the limbs and face, hypotonia, and developmental delay
GUncertain significance
NALCN
Single nucleotide variant
(splice donor variant)
Congenital contractures of the limbs and face, hypotonia, and developmental delay
GUncertain significance
NALCN
(A310T)
Single nucleotide variant
(missense variant)
Congenital contractures of the limbs and face, hypotonia, and developmental delay
GLikely benign
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