Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.47351134G>CCA376674213RBP3c.2650G>C (p.Val884Leu)
 ClinVar dbSNP
10g.47351134G>ACA200431RBP3c.2650G>A (p.Val884Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched