Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.763901A>G	CA339795	SLC52A3	c.670T>C (p.Phe224Leu) c.567+1307T>C (n.567+1307T>C) n.618+1307T>C	ClinVar dbSNP gnomAD v4
20	g.763901A=	CA2345349444	SLC52A3	c.670T= (p.Phe224=) c.567+1307T= (n.567+1307T=) n.618+1307T=	dbSNP

Number of alleles fetched