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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NONO
(K68fs)
Microsatellite
(frameshift variant +1 more)
Syndromic X-linked intellectual disability 34
GPathogenic
NONO
(F5fs +1 more)
Deletion
(frameshift variant)
Syndromic X-linked intellectual disability 34
GPathogenic
NONO
(P148fs +1 more)
Deletion
(frameshift variant)
Neurodevelopmental delay
GPathogenic
NONO
(P36L)
Single nucleotide variant
(missense variant +1 more)
Syndromic X-linked intellectual disability 34
GUncertain significance
NONO
(R181C +1 more)
Single nucleotide variant
(missense variant)
Mild global developmental delay
GUncertain significance
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