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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CA5A
Deletion
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
GPathogenic
CA5A
(M28K)
Single nucleotide variant
(missense variant +1 more)
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
GUncertain significance
CA5A
(Q194*)
Single nucleotide variant
(nonsense +1 more)
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
GLikely pathogenic
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