Allele Registry

Canonical Allele Identifier: PA2830508770

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Leu669Val	CA409806217 NM_201413.3:c.2005T>G