Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.7267833A>GCA124253INSRc.164T>C (p.Val55Ala)
n.139T>C
c.242T>C (p.Val81Ala)
 ClinVar dbSNP gnomAD v4
19g.7267833A=CA2320836559INSRc.164T= (p.Val55=)
n.139T=
c.242T= (p.Val81=)
 dbSNP

Number of alleles fetched