Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.134493586G>TCA120896HPRT1c.481G>T (p.Ala161Ser)
n.639G>T
n.439G>T
c.499G>T (p.Ala167Ser)
 ClinVar dbSNP COSMIC
Xg.134493586G>ACA414714591HPRT1c.481G>A (p.Ala161Thr)
n.639G>A
n.439G>A
c.499G>A (p.Ala167Thr)
 ClinVar dbSNP gnomAD v4

Number of alleles fetched