Allele Registry

Canonical Allele Identifier: PA2825818511

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001141462

ClinVar Variation:

897923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Lys669Asn	CA409805496 NM_001136130.2:c.2007G>T CA409805497 NM_001136130.2:c.2007G>C