Allele Registry

Canonical Allele Identifier: PA2830508984

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019717

RCV000019718

RCV000020306

RCV000084561

ClinVar Variation:

18091

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Ala617Gly	CA127794 NM_201414.3:c.1850C>G