Canonical Allele Identifier: PA2825808572
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 1298879
ClinVar RCV Id: RCV001727209
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Ile692Met
CA409805552
NM_001136016.3:c.2076C>G