Canonical Allele Identifier: PA2830508773
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18099
ClinVar RCV Id: RCV000019727 RCV000084562
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Glu674Lys
CA127802
NM_201413.3:c.2020G>A