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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDK5RAP2
Single nucleotide variant
(splice acceptor variant)
Microcephaly 3, primary, autosomal recessive
+1 more
GPathogenic
CDK5RAP2
Single nucleotide variant
(splice acceptor variant)
Microcephaly 3, primary, autosomal recessive
GLikely pathogenic
CDK5RAP2
Deletion
(nonsense +1 more)
Microcephaly 3, primary, autosomal recessive
GLikely pathogenic
CDK5RAP2
(E273K)
Single nucleotide variant
(missense variant +1 more)
Microcephaly 3, primary, autosomal recessive
GUncertain significance
CDK5RAP2
(R150Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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