Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.100407484G>A	CA316336	PCDH19	c.1114C>T (p.Arg372Trp)	ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
X	g.100407484G=	CA2447976739	PCDH19	c.1114C= (p.Arg372=)	dbSNP

Number of alleles fetched