Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
14	g.67727097C>T	CA252078	GPHN,RDH12	c.565C>T (p.Gln189Ter) c.1313-8098C>T (n.1313-8098C>T)	ClinVar dbSNP
14	g.67727097C=	CA2144003459	GPHN,RDH12	c.565C= (p.Gln189=) c.1313-8098C= (n.1313-8098C=)	dbSNP

Number of alleles fetched