Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583358A>GCA216827KRT14c.1151T>C (p.Leu384Pro)
n.98T>C
n.601T>C
 ClinVar dbSNP
17g.41583358A=CA2260085369KRT14c.1151T= (p.Leu384=)
n.98T=
n.601T=
 dbSNP

Number of alleles fetched