Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6044361G>A	CA114135	VWF	c.2372C>T (p.Thr791Met) n.421-50427C>T	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12	g.6044361G=	CA2013884563	VWF	c.2372C= (p.Thr791=) n.421-50427C=	dbSNP

Number of alleles fetched