Allele Registry

Canonical Allele Identifier: PA2825808462

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Thr639Met	CA9987104 NM_001136016.3:c.1916C>T