Allele Registry

Canonical Allele Identifier: PA2825817946

Gene: APP HGNC NCBI

ClinVar Allele:

33130

ClinVar RCV:

RCV000019717

RCV000019718

RCV000020306

RCV000084561

ClinVar Variation:

18091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Ala561Gly	CA127794 NM_001136129.3:c.1682C>G