Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41624247A>GCA216606KRT17c.263T>C (p.Met88Thr)
c.-312-41T>C (n.-312-41T>C)
n.329T>C
n.50T>C
c.58T>C (p.Cys20Arg)
c.218T>C (p.Met73Thr)
ClinVar dbSNP
17g.41624247A>TCA216605KRT17c.263T>A (p.Met88Lys)
c.-312-41T>A (n.-312-41T>A)
n.329T>A
n.50T>A
c.58T>A (p.Cys20Ser)
c.218T>A (p.Met73Lys)
ClinVar dbSNP
17g.41624247A=CA2260105476KRT17c.263T= (p.Met88=)
c.-312-41T= (n.-312-41T=)
n.329T=
n.50T=
c.58T= (p.Cys20=)
c.218T= (p.Met73=)
dbSNP

Number of alleles fetched