Allele Registry

Canonical Allele Identifier: PA2826270356

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Lys669Asn	CA409806220 NM_001204301.2:c.2007A>T CA409806222 NM_001204301.2:c.2007A>C