Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225620G>T	CA124904	HBB	c.422C>A (p.Ala141Asp) c.238C>A (n.238C>A)	ClinVar dbSNP
11	g.5225620G>A	CA125422	HBB	c.422C>T (p.Ala141Val) c.238C>T (n.238C>T)	ClinVar dbSNP

Number of alleles fetched