Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6072369G>T	CA114174	VWF	c.1071C>A (p.Tyr357Ter) n.420+38146C>A	ClinVar dbSNP
12	g.6072369G=	CA2013897849	VWF	c.1071C= (p.Tyr357=) n.420+38146C=	dbSNP

Number of alleles fetched