Canonical Allele Identifier: PA2826270365
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 1912162
ClinVar RCV Id: RCV002578767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Ile684Met
CA409805627
NM_001204301.2:c.2052C>G