Allele Registry

Canonical Allele Identifier: PA2825818000

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019715

RCV000815476

RCV002054452

ClinVar Variation:

18089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Val586Phe	CA127792 NM_001136129.3:c.1756G>T