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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNTNAP4
(E148K +4 more)
Single nucleotide variant
(missense variant +2 more)
CNTNAP4-related disorder
GUncertain significance
CNTNAP4
(Q268R +6 more)
Single nucleotide variant
(missense variant +2 more)
CNTNAP4-related disorder
GLikely benign
CNTNAP4
(F134Y +8 more)
Single nucleotide variant
(missense variant +1 more)
CNTNAP4-related disorder
GLikely benign
CNTNAP4
(I364F +8 more)
Single nucleotide variant
(missense variant +1 more)
CNTNAP4-related disorder
GLikely benign
CNTNAP4
(R1036S +9 more)
Single nucleotide variant
(missense variant +1 more)
CNTNAP4-related disorder
GUncertain significance
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