Allele Registry

Canonical Allele Identifier: PA2825817942

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Leu557Val	CA409806217 NM_001136129.3:c.1669T>G