Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.93600470C>ACA377617449FFAR4,RBP4c.278G>T (p.Gly93Val)
c.272G>T (p.Gly91Val)
c.697-3604C>A (n.697-3604C>A)
ClinVar dbSNP
10g.93600470C>TCA122833FFAR4,RBP4c.278G>A (p.Gly93Asp)
c.272G>A (p.Gly91Asp)
c.697-3604C>T (n.697-3604C>T)
ClinVar dbSNP

Number of alleles fetched