Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.52646748C>ACA120290KRT2c.1461G>T (p.Glu487Asp)
 ClinVar dbSNP
12g.52646748C>TCA6585476KRT2c.1461G>A (p.Glu487=)
 dbSNP ExAC gnomAD v2

Number of alleles fetched