Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6021960C>A	CA228427	VWF	c.3614G>T (p.Arg1205Leu) n.421-28026G>T	ClinVar dbSNP
12	g.6021960C>T	CA114160	VWF	c.3614G>A (p.Arg1205His) n.421-28026G>A	ClinVar dbSNP gnomAD v4
12	g.6021960C=	CA2013874091	VWF	c.3614G= (p.Arg1205=) n.421-28026G=	dbSNP

Number of alleles fetched