Allele Registry

Canonical Allele Identifier: PA2825808504

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Lys663Asn	CA409806220 NM_001136016.3:c.1989A>T CA409806222 NM_001136016.3:c.1989A>C