Allele Registry

Canonical Allele Identifier: PA2825818852

Gene: APP HGNC NCBI

ClinVar Allele:

33132

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Lys560_Met561delinsAsnLeu	CA127795 NM_001136131.2:c.1680_1681delinsTC