Allele Registry

Canonical Allele Identifier: PA127806

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019729

RCV000084564

RCV000687111

ClinVar Variation:

18101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Asp584Asn	CA127804 NM_001136131.2:c.1750G>A