Canonical Allele Identifier: PA2825818499
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Val661Gly
CA127793
NM_001136130.2:c.1982T>G