Allele Registry

Canonical Allele Identifier: PA2825808506

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Leu664Val	CA409806217 NM_001136016.3:c.1990T>G