Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699655T>G	CA145403	PRNP	c.435T>G (p.Tyr145Ter) c.124T>G (n.124T>G)	ClinVar dbSNP
20	g.4699655T=	CA2347156547	PRNP	c.435T= (p.Tyr145=) c.124T= (n.124T=)	dbSNP

Number of alleles fetched