Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
3	g.10142139T>C	CA020246	VHL	c.292T>C (p.Tyr98His)	ClinVar dbSNP gnomAD v2 gnomAD v4
3	g.10142139T>A	CA351750883	VHL	c.292T>A (p.Tyr98Asn)	ClinVar dbSNP COSMIC
3	g.10142139T=	CA1345066250	VHL	c.292T= (p.Tyr98=)	dbSNP

Number of alleles fetched