Allele Registry

Canonical Allele Identifier: PA2826270620

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Lys633_Met634delinsAsnLeu	CA127795 NM_001204302.2:c.1899_1900delinsTC