Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.68781784G>ACA344962CPT1Ac.1339C>T (p.Arg447Ter)
c.1435C>T (p.Arg479Ter)
 ClinVar dbSNP gnomAD v4
11g.68781784G=CA3182733453CPT1Ac.1339C= (p.Arg447=)
c.1435C= (p.Arg479=)
 dbSNP

Number of alleles fetched