Allele Registry

Canonical Allele Identifier: PA2830508791

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019724

RCV000084570

RCV003509483

ClinVar Variation:

18097

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Val696Met	CA127800 NM_201413.3:c.2086G>A