Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.47448079G>T	CA199511	RAPSN	c.264C>A (p.Asn88Lys)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11	g.47448079G=	CA1969378565	RAPSN	c.264C= (p.Asn88=)	dbSNP
11	g.47448079G>C	CA380334837	RAPSN	c.264C>G (p.Asn88Lys)	ClinVar dbSNP

Number of alleles fetched