Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.7267555T>ACA124259INSRc.442A>T (p.Lys148Ter)
n.417A>T
c.520A>T (p.Lys174Ter)
 ClinVar dbSNP
19g.7267555T=CA2320836457INSRc.442A= (p.Lys148=)
n.417A=
c.520A= (p.Lys174=)
 dbSNP

Number of alleles fetched