Allele Registry

Canonical Allele Identifier: PA2828960813

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Leu632Val	CA409806217 NM_001385253.1:c.1894T>G