Allele Registry

Canonical Allele Identifier: PA113639

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019715

RCV000815476

RCV002054452

ClinVar Variation:

18089

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Val717Phe	CA127792 NM_000484.4:c.2149G>T