"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 374123	NM_000018.4(ACADVL):c.1358G>A (p.Arg453Gln)	ACADVL (R453Q +3 more)	Single nucleotide variant (missense variant)	Very long chain acyl-CoA dehydrogenase deficiency	GLikely pathogenic FDA Recognized database
Select item 203585	NM_000018.4(ACADVL):c.1376G>A (p.Arg459Gln)	ACADVL (R459Q +3 more)	Single nucleotide variant (missense variant)	Very long chain acyl-CoA dehydrogenase deficiency	GPathogenic FDA Recognized database