Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.1220627G>CCA402949588STK11c.644G>C (p.Gly215Ala)
c.272G>C (p.Gly91Ala)
c.470G>C (p.Gly157Ala)
n.542G>C
n.734G>C
n.615G>C
c.422G>C (p.Gly141Ala)
n.1269G>C
dbSNP COSMIC COSMIC
19g.1220627G>ACA16603147STK11c.644G>A (p.Gly215Asp)
c.272G>A (p.Gly91Asp)
c.470G>A (p.Gly157Asp)
n.542G>A
n.734G>A
n.615G>A
c.422G>A (p.Gly141Asp)
n.1269G>A
ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched