Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.66435221T>GCA134601MAP2K1c.209T>G (p.Leu70Arg)
c.275T>G (p.Leu92Arg)
n.711T>G
n.786T>G
 ClinVar dbSNP
15g.66435221T=CA2184071776MAP2K1c.209T= (p.Leu70=)
c.275T= (p.Leu92=)
n.711T=
n.786T=
 dbSNP

Number of alleles fetched