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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLAA
(P630I +1 more)
Indel
(missense variant)
Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies
+1 more
GUncertain significance
PLAA
(I356M)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies
+2 more
GUncertain significance
PLAA
(P346T)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies
GUncertain significance
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