Canonical Allele Identifier: PA2825808589
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Val693Gly
CA127793
NM_001136016.3:c.2078T>G