Allele Registry

Canonical Allele Identifier: PA2825817994

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019723

RCV000084573

RCV001947096

ClinVar Variation:

18096

1457308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Ile585Val	CA127799 NM_001136129.3:c.1753A>G CA2573157339 NM_001136129.3:c.1752_1753delinsTG