Canonical Allele Identifier: PA2826270660
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Val680Gly
CA127793
NM_001204302.2:c.2039T>G