Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.156876526A>TCA342938642NTRK1c.1579A>T (p.Met527Leu)
c.*351A>T (n.*351A>T)
c.1759A>T (p.Met587Leu)
c.1750A>T (p.Met584Leu)
c.1741A>T (p.Met581Leu)
c.1651A>T (p.Met551Leu)
n.2212A>T
dbSNP
1g.156876526A>GCA256300NTRK1c.1579A>G (p.Met527Val)
c.*351A>G (n.*351A>G)
c.1759A>G (p.Met587Val)
c.1750A>G (p.Met584Val)
c.1741A>G (p.Met581Val)
c.1651A>G (p.Met551Val)
n.2212A>G
ClinVar dbSNP

Number of alleles fetched