Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.29222404A>TCA346463324ALKc.3455T>A (p.Leu1152Gln)
c.682T>A
n.332T>A
c.251T>A (p.Leu84Gln)
c.335T>A (p.Leu112Gln)
c.149T>A (p.Leu50Gln)
c.2324T>A (p.Leu775Gln)
c.608T>A (p.Leu203Gln)
dbSNP
2g.29222404A>CCA16602594ALKc.3455T>G (p.Leu1152Arg)
c.682T>G
n.332T>G
c.251T>G (p.Leu84Arg)
c.335T>G (p.Leu112Arg)
c.149T>G (p.Leu50Arg)
c.2324T>G (p.Leu775Arg)
c.608T>G (p.Leu203Arg)
ClinVar dbSNP COSMIC
2g.29222404A>GCA346463323ALKc.3455T>C (p.Leu1152Pro)
c.682T>C
n.332T>C
c.251T>C (p.Leu84Pro)
c.335T>C (p.Leu112Pro)
c.149T>C (p.Leu50Pro)
c.2324T>C (p.Leu775Pro)
c.608T>C (p.Leu203Pro)
dbSNP

Number of alleles fetched