Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102852847T>ACA229782PAHc.810A>T (p.Arg270Ser)
c.795A>T (p.Arg265Ser)
n.569A>T
 ClinVar dbSNP
12g.102852847T=CA2059446273PAHc.810A= (p.Arg270=)
c.795A= (p.Arg265=)
n.569A=
 dbSNP

Number of alleles fetched