Canonical Allele Identifier: PA2830509010
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958817.1:p.Val642Gly
CA127793
NM_201414.3:c.1925T>G