Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41586438C>GCA216939KRT14c.397G>C (p.Val133Leu)
ClinVar dbSNP
17g.41586438C>TCA216937KRT14c.397G>A (p.Val133Met)
ClinVar dbSNP COSMIC
17g.41586438C>ACA216941KRT14c.397G>T (p.Val133Leu)
ClinVar dbSNP

Number of alleles fetched