Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699813T>C	CA256779	PRNP	c.593T>C (p.Phe198Ser) c.282T>C (n.282T>C)	ClinVar dbSNP
20	g.4699813T=	CA2347156623	PRNP	c.593T= (p.Phe198=) c.282T= (n.282T=)	dbSNP

Number of alleles fetched