C4540052[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 771448	NM_001144869.3(LIPT2):c.690C>T (p.Pro230=)	LIPT2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1601557	NM_001144869.3(LIPT2):c.273C>T (p.Phe91=)	LIPT2, LIPT2-AS1	Single nucleotide variant (non-coding transcript variant +2 more)	not provided +1 more	GBenign/Likely benign