Allele Registry

Canonical Allele Identifier: PA127811

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019729

RCV000084564

RCV000687111

ClinVar Variation:

18101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Asp670Asn	CA127804 NM_001136016.3:c.2008G>A