Allele Registry

Canonical Allele Identifier: PA2828960851

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019715

RCV000815476

RCV002054452

ClinVar Variation:

18089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Val661Phe	CA127792 NM_001385253.1:c.1981G>T