Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.63493155C>GCA200125EEF1A2c.754G>C (p.Asp252His)
n.3323G>C
c.*626G>C (n.*626G>C)
 ClinVar dbSNP
20g.63493155C>TCA409648631EEF1A2c.754G>A (p.Asp252Asn)
n.3323G>A
c.*626G>A (n.*626G>A)
 ClinVar dbSNP

Number of alleles fetched