Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41571524T>CCA115908KRT9c.469A>G (p.Met157Val)
c.-189-42A>G (n.-189-42A>G)
 ClinVar dbSNP
17g.41571524T>GCA290680164KRT9c.469A>C (p.Met157Leu)
c.-189-42A>C (n.-189-42A>C)
 dbSNP gnomAD v4

Number of alleles fetched