Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6044322C>A	CA114168	VWF	c.2411G>T (p.Cys804Phe) n.421-50388G>T	ClinVar dbSNP
12	g.6044322C=	CA2013884545	VWF	c.2411G= (p.Cys804=) n.421-50388G=	dbSNP

Number of alleles fetched