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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCLO
(I4249T)
Single nucleotide variant
(missense variant)
Pontocerebellar hypoplasia type 3
+1 more
GUncertain significance
PCLO
(R2056K)
Single nucleotide variant
(missense variant)
Pontocerebellar hypoplasia type 3
+2 more
GConflicting classifications of pathogenicity
PCLO
(G1716V)
Single nucleotide variant
(missense variant)
Pontocerebellar hypoplasia type 3
GUncertain significance
PCLO
(T1617A)
Single nucleotide variant
(missense variant)
Pontocerebellar hypoplasia type 3
GUncertain significance
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