Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.47447859C>T	CA119258	RAPSN	c.484G>A (p.Glu162Lys)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11	g.47447859C=	CA1969390445	RAPSN	c.484G= (p.Glu162=)	dbSNP

Number of alleles fetched