Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.47447819T>C	CA351333	RAPSN	c.524A>G (p.Gln175Arg)	ClinVar dbSNP gnomAD v4
11	g.47447819T=	CA1969390425	RAPSN	c.524A= (p.Gln175=)	dbSNP
11	g.47447819T>G	CA380333564	RAPSN	c.524A>C (p.Gln175Pro)	dbSNP gnomAD v4

Number of alleles fetched