Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.52488346A>CCA124170KRT6Ac.1406T>G (p.Leu469Arg)
 ClinVar dbSNP
12g.52488346A>GCA170745KRT6Ac.1406T>C (p.Leu469Pro)
 ClinVar dbSNP
12g.52488346A=CA2036520308KRT6Ac.1406T= (p.Leu469=)
 dbSNP

Number of alleles fetched