Allele Registry

Canonical Allele Identifier: PA2830508769

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Lys668Asn	CA409806220 NM_201413.3:c.2004A>T CA409806222 NM_201413.3:c.2004A>C