Canonical Allele Identifier: PA2826270372
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Ala695Thr
CA090906
NM_001204301.2:c.2083G>A