Allele Registry

Canonical Allele Identifier: PA2826270357

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Leu670Val	CA409806217 NM_001204301.2:c.2008T>G