Allele Registry

Canonical Allele Identifier: PA2828960787

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Lys614_Met615delinsAsnLeu	CA127795 NM_001385253.1:c.1842_1843delinsTC