Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.11881049G>ACA16620660GNALc.1291G>A (p.Val431Met)
c.1060G>A (p.Val354Met)
c.439G>A (p.Val147Met)
ClinVar dbSNP COSMIC
18g.11881049G=CA2284983272GNALc.1291G= (p.Val431=)
c.1060G= (p.Val354=)
c.439G= (p.Val147=)
dbSNP

Number of alleles fetched