Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225603G>C	CA124910	HBB	c.439C>G (p.His147Asp) c.255C>G (n.255C>G)	ClinVar dbSNP
11	g.5225603G>A	CA125478	HBB	c.439C>T (p.His147Tyr) c.255C>T (n.255C>T)	ClinVar dbSNP

Number of alleles fetched