Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.153740638C>T	CA10550293	ABCD1	c.1699C>T (p.Gln567Ter) n.2171C>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
X	g.153740638C=	CA2466456614	ABCD1	c.1699C= (p.Gln567=) n.2171C=	dbSNP

Number of alleles fetched