Allele Registry

Canonical Allele Identifier: PA2826270344

Gene: APP HGNC NCBI

ClinVar Allele:

33132

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Lys652_Met653delinsAsnLeu	CA127795 NM_001204301.2:c.1956_1957delinsTC