Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.52552656A>CCA163414KRT71c.422T>G (p.Phe141Cys)
c.176T>G (p.Phe59Cys)
 ClinVar dbSNP
12g.52552656A=CA2036551655KRT71c.422T= (p.Phe141=)
c.176T= (p.Phe59=)
 dbSNP

Number of alleles fetched