Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.152858816C>TCA341090NSDHLc.314C>T (p.Ala105Val)
c.362C>T (p.Ala121Val)
 ClinVar dbSNP
Xg.152858816C=CA2466151264NSDHLc.314C= (p.Ala105=)
c.362C= (p.Ala121=)
 dbSNP

Number of alleles fetched