Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.165755015G>ACA119087GALNT3c.1441C>T (p.Gln481Ter)
c.655C>T (p.Gln219Ter)
n.1717C>T
 ClinVar dbSNP COSMIC
2g.165755015G=CA1304731342GALNT3c.1441C= (p.Gln481=)
c.655C= (p.Gln219=)
n.1717C=
 dbSNP

Number of alleles fetched