Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.3083156C>ACA121948AVPc.143G>T (p.Gly48Val)
ClinVar dbSNP gnomAD v4
20g.3083156C>GCA408061849AVPc.143G>C (p.Gly48Ala)
dbSNP
20g.3083156C=CA2346405601AVPc.143G= (p.Gly48=)
dbSNP

Number of alleles fetched