Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.52488338C>TCA124169KRT6Ac.1414G>A (p.Glu472Lys)
ClinVar dbSNP
12g.52488338C=CA2036520302KRT6Ac.1414G= (p.Glu472=)
dbSNP
12g.52488338C>GCA384953286KRT6Ac.1414G>C (p.Glu472Gln)
dbSNP

Number of alleles fetched