Allele Registry

Canonical Allele Identifier: PA2828960850

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019723

RCV000084573

RCV001947096

ClinVar Variation:

18096

1457308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Ile660Val	CA127799 NM_001385253.1:c.1978A>G CA2573157339 NM_001385253.1:c.1977_1978delinsTG