Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
14	g.67726086G>T	CA252083	GPHN,RDH12	c.379G>T (p.Gly127Ter) c.1313-9109G>T (n.1313-9109G>T)	ClinVar dbSNP
14	g.67726086G=	CA2144003017	GPHN,RDH12	c.379G= (p.Gly127=) c.1313-9109G= (n.1313-9109G=)	dbSNP

Number of alleles fetched