Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6057995T>C	CA114178	VWF	c.1583A>G (p.Asn528Ser) n.420+52520A>G	ClinVar dbSNP ExAC gnomAD v2
12	g.6057995T=	CA2013892198	VWF	c.1583A= (p.Asn528=) n.420+52520A=	dbSNP

Number of alleles fetched