Canonical Allele Identifier: PA2830508798
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Val698Gly
CA127793
NM_201413.3:c.2093T>G