Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225609T>A	CA038142	HBB	c.433A>T (p.Lys145Ter) c.249A>T (n.249A>T)	ClinVar dbSNP
11	g.5225609T>C	CA125032	HBB	c.433A>G (p.Lys145Glu) c.249A>G (n.249A>G)	ClinVar dbSNP

Number of alleles fetched