Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.131583392G>CCA339974ARG1,MED23c.703G>C (p.Gly235Arg)
c.727G>C (p.Gly243Arg)
c.4077+4317C>G (p.=)
c.4095+4317C>G (p.=)
c.448G>C (p.Gly150Arg)
n.687G>C
ClinVar dbSNP
6g.131583392G>ACA3999348ARG1,MED23c.703G>A (p.Gly235Arg)
c.727G>A (p.Gly243Arg)
c.4077+4317C>T (p.=)
c.4095+4317C>T (p.=)
c.448G>A (p.Gly150Arg)
n.687G>A
ClinVar dbSNP ExAC gnomAD COSMIC

Number of alleles fetched