Allele Registry

Canonical Allele Identifier: PA2826270367

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019731

RCV000084565

RCV003987327

ClinVar Variation:

18103

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Leu687Val	CA127815 NM_001204301.2:c.2059C>G