Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.792340C>ACA115174SLC25A22c.706G>T (p.Gly236Trp)
c.781G>T (p.Gly261Trp)
 ClinVar dbSNP
11g.792340C=CA1947288367SLC25A22c.706G= (p.Gly236=)
c.781G= (p.Gly261=)
 dbSNP

Number of alleles fetched