Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6022833A>G	CA228410	VWF	c.3445T>C (p.Cys1149Arg) n.421-28899T>C	ClinVar dbSNP gnomAD v4
12	g.6022833A=	CA2013874480	VWF	c.3445T= (p.Cys1149=) n.421-28899T=	dbSNP

Number of alleles fetched