Allele Registry

Canonical Allele Identifier: PA2825818488

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019723

RCV000084573

RCV001947096

ClinVar Variation:

18096

1457308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Ile660Val	CA127799 NM_001136130.2:c.1978A>G CA2573157339 NM_001136130.2:c.1977_1978delinsTG