Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.78955486A>GCA114602ARSBc.707T>C (p.Leu236Pro)
n.778T>C
ClinVar dbSNP gnomAD v4
5g.78955486A=CA1557697770ARSBc.707T= (p.Leu236=)
n.778T=
dbSNP

Number of alleles fetched