Canonical Allele Identifier: PA2830508793
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18096
ClinVar Variation Id: 1457308
ClinVar RCV Id: RCV001947096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Ile697Val
CA127799
NM_201413.3:c.2089A>G
CA2573157339
NM_201413.3:c.2088_2089delinsTG