Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226996T>G	CA130022	HBB	c.26A>C (p.Lys9Thr) n.77A>C	ClinVar dbSNP
11	g.5226996T>C	CA125468	HBB	c.26A>G (p.Lys9Arg) n.77A>G	ClinVar dbSNP
11	g.5226996T>A	CA125428	HBB	c.26A>T (p.Lys9Met) n.77A>T	ClinVar dbSNP

Number of alleles fetched