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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCNT
(R1239H +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PCNT
(A2011V +1 more)
Single nucleotide variant
(missense variant)
PCNT-related disorder
+2 more
GConflicting classifications of pathogenicity
PCNT
(V1952M +1 more)
Single nucleotide variant
(missense variant)
Microcephaly
GUncertain significance
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