Allele Registry

Canonical Allele Identifier: PA2826270921

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019715

RCV000815476

RCV002054452

ClinVar Variation:

18089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Val624Phe	CA127792 NM_001204303.2:c.1870G>T