Allele Registry

Canonical Allele Identifier: PA2826270920

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019733

RCV000518713

ClinVar Variation:

18105

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Val624Leu	CA127816 NM_001204303.2:c.1870G>C