Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
8	g.118932982A>G	CA118569	TNFRSF11B	c.349T>C (p.Phe117Leu)	ClinVar dbSNP gnomAD v3 gnomAD v4
8	g.118932982A=	CA1814470976	TNFRSF11B	c.349T= (p.Phe117=)	dbSNP

Number of alleles fetched