Allele Registry

Canonical Allele Identifier: PA2830508760

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Ala654Val	CA258118 NM_201413.3:c.1961C>T