Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
6	g.79916658T>C	CA179999	ELOVL4	c.895A>G (p.Met299Val)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6	g.79916658T=	CA1640822793	ELOVL4	c.895A= (p.Met299=)	dbSNP

Number of alleles fetched