Allele Registry

Canonical Allele Identifier: PA2825808476

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019720

RCV000034924

RCV000084589

RCV003390694

ClinVar Variation:

18093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Lys646_Met647delinsAsnLeu	CA127795 NM_001136016.3:c.1938_1939delinsTC