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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACADVL, LOC130060113
Single nucleotide variant
(5 prime UTR variant +1 more)
Very long chain acyl-CoA dehydrogenase deficiency
+1 more
GLikely benign
ACADVL, LOC130060113
(R23Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Very long chain acyl-CoA dehydrogenase deficiency
GBenign
ACADVL, LOC130060113
(G43D +1 more)
Single nucleotide variant
(missense variant +1 more)
Very long chain acyl-CoA dehydrogenase deficiency
GBenign
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