Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.111787039C>TCA200132KCND3c.1174G>A (p.Val392Ile)
 ClinVar dbSNP
1g.111787039C=CA1189065703KCND3c.1174G= (p.Val392=)
 dbSNP

Number of alleles fetched