Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.74521008C>ACA272495SLC16A2c.449C>A (p.Ala150Glu)
c.358C>A
 ClinVar dbSNP
Xg.74521008C>TCA222962SLC16A2c.449C>T (p.Ala150Val)
c.358C>T
 ClinVar dbSNP

Number of alleles fetched