C1832916[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1334090	NM_000719.7(CACNA1C):c.2451del (p.Ala818fs)	CACNA1C (A815fs +1 more)	Deletion (frameshift variant)	Timothy syndrome	GLikely pathogenic
Select item 1334091	NM_000719.7(CACNA1C):c.5445-496G>A	CACNA1C, CACNA1C-AS1 (R1850K +1 more)	Single nucleotide variant (missense variant +1 more)	Timothy syndrome	GUncertain significance