Allele Registry

Canonical Allele Identifier: PA2830508968

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Lys595_Met596delinsAsnLeu	CA127795 NM_201414.3:c.1785_1786delinsTC