Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.55223902C>GCA117892RAB27An.2490G>C
c.454G>C (p.Ala152Pro)
n.2622G>C
ClinVar dbSNP
15g.55223902C>TCA392529511RAB27An.2490G>A
c.454G>A (p.Ala152Thr)
n.2622G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched