Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225614G>A	CA037606	HBB	c.428C>T (p.Ala143Val) c.244C>T (n.244C>T)	dbSNP
11	g.5225614G>T	CA125074	HBB	c.428C>A (p.Ala143Asp) c.244C>A (n.244C>A)	ClinVar dbSNP

Number of alleles fetched