Allele Registry

Canonical Allele Identifier: PA113527

Gene: APP HGNC NCBI

MaveDb:

Score 0.0134113316

Score -0.0183079368

ClinVar RCV:

RCV000084560

ClinVar Variation:

98236

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Asp678Asn	CA225504 NM_000484.4:c.2032G>A