Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.78117385A>TCA120836PGK1c.491A>T (p.Asp164Val)
c.407A>T (p.Asp136Val)
n.483A>T
 ClinVar dbSNP
Xg.78117385A=CA2439138338PGK1c.491A= (p.Asp164=)
c.407A= (p.Asp136=)
n.483A=
 dbSNP

Number of alleles fetched