Allele Registry

Canonical Allele Identifier: PA2830508784

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084567

RCV001141463

ClinVar Variation:

98237

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Ala694Val	CA225505 NM_201413.3:c.2081C>T