Allele Registry

Canonical Allele Identifier: PA2825818440

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Leu632Val	CA409806217 NM_001136130.2:c.1894T>G