Allele Registry

Canonical Allele Identifier: PA2830508793

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019723

RCV000084573

RCV001947096

ClinVar Variation:

18096

1457308

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Ile697Val	CA127799 NM_201413.3:c.2089A>G CA2573157339 NM_201413.3:c.2088_2089delinsTG