Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.36662954T>CCA123445PAX9c.62T>C (p.Leu21Pro)
c.-500T>C (n.-500T>C)
n.364T>C
 ClinVar dbSNP
14g.36662954T=CA2129502288PAX9c.62T= (p.Leu21=)
c.-500T= (n.-500T=)
n.364T=
 dbSNP

Number of alleles fetched