Canonical Allele Identifier: PA2830508770
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 932452
ClinVar RCV Id: RCV001200266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Leu669Val
CA409806217
NM_201413.3:c.2005T>G