Allele Registry

Canonical Allele Identifier: PA2830508974

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Ala598Val	CA258118 NM_201414.3:c.1793C>T