Canonical Allele Identifier: PA2830508800
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Val698Leu
CA127816
NM_201413.3:c.2092G>C