Canonical Allele Identifier: PA2825808548
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Thr690Ala
CA127814
NM_001136016.3:c.2068A>G