"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CLPP"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 453066	NM_006012.4(CLPP):c.520C>T (p.Arg174Cys)	CLPP (R174C)	Single nucleotide variant (missense variant)	Perrault syndrome 3 +1 more	GUncertain significance
Select item 1208030	NM_006012.4(CLPP):c.555+16G>A	CLPP	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign