Allele Registry

Canonical Allele Identifier: PA2826270877

Gene: APP HGNC NCBI

ClinVar Allele:

33132

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Lys577_Met578delinsAsnLeu	CA127795 NM_001204303.2:c.1731_1732delinsTC