Canonical Allele Identifier: PA2825817942
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 932452
ClinVar RCV Id: RCV001200266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Leu557Val
CA409806217
NM_001136129.3:c.1669T>G