Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6019479C>G	CA114121	VWF	c.3939G>C (p.Trp1313Cys) n.421-25545G>C	ClinVar dbSNP
12	g.6019479C=	CA2013873004	VWF	c.3939G= (p.Trp1313=) n.421-25545G=	dbSNP

Number of alleles fetched