Allele Registry

Canonical Allele Identifier: PA2830509009

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019733

RCV000518713

ClinVar Variation:

18105

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Val642Leu	CA127816 NM_201414.3:c.1924G>C