Allele Registry

Canonical Allele Identifier: PA2830509012

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019715

RCV000815476

RCV002054452

ClinVar Variation:

18089

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Val642Phe	CA127792 NM_201414.3:c.1924G>T