Allele Registry

Canonical Allele Identifier: PA127807

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019729

RCV000084564

RCV000687111

ClinVar Variation:

18101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Asp601Asn	CA127804 NM_001204303.2:c.1801G>A