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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCLO
(R4722Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(S3582T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(A2867S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(P1895S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(E1576Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(V1139F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(A991T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(M642I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
PCLO
(P456S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PCLO
(G406E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
PCLO
(P73Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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