Allele Registry

Canonical Allele Identifier: PA127796

Gene: APP HGNC NCBI

ClinVar Allele:

33132

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Lys670_Met671delinsAsnLeu	CA127795 NM_000484.4:c.2010_2011delinsTC