Allele Registry

Canonical Allele Identifier: PA113559

Gene: APP HGNC NCBI

MaveDb:

Score 0.0202005284

Score -0.0699830022

ClinVar RCV:

RCV000019727

RCV000084562

ClinVar Variation:

18099

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Glu693Lys	CA127802 NM_000484.4:c.2077G>A