Allele Registry

Canonical Allele Identifier: PA2830508799

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019715

RCV000815476

RCV002054452

ClinVar Variation:

18089

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Val698Phe	CA127792 NM_201413.3:c.2092G>T