Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699698C>T	CA145405	PRNP	c.478C>T (p.Gln160Ter) c.167C>T (n.167C>T)	ClinVar dbSNP
20	g.4699698C=	CA2347156566	PRNP	c.478C= (p.Gln160=) c.167C= (n.167C=)	dbSNP

Number of alleles fetched