Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41571512T>ACA115905KRT9c.481A>T (p.Asn161Tyr)
c.-189-30A>T (n.-189-30A>T)
 ClinVar dbSNP
17g.41571512T>GCA216559KRT9c.481A>C (p.Asn161His)
c.-189-30A>C (n.-189-30A>C)
 ClinVar dbSNP

Number of alleles fetched