Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.18594338A>CCA342059CRLF1c.1121T>G (p.Leu374Arg)
n.98T>G
c.1055T>G (p.Leu352Arg)
 ClinVar dbSNP
19g.18594338A=CA2326431051CRLF1c.1121T= (p.Leu374=)
n.98T=
c.1055T= (p.Leu352=)
 dbSNP

Number of alleles fetched