Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.165046998A>CCA115005SIc.1730T>G (p.Val577Gly)
c.1631T>G (p.Val544Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.165046998A>GCA355052434SIc.1730T>C (p.Val577Ala)
c.1631T>C (p.Val544Ala)
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched