Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.49524145C>TCA9903505PTGISc.768G>A (p.Leu256=)
n.589G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.49524145C>ACA315139771PTGISc.768G>T (p.Leu256=)
n.589G>T
dbSNP
20g.49524145C>GCA315139772PTGISc.768G>C (p.Leu256=)
n.589G>C
dbSNP

Number of alleles fetched