Allele Registry

Canonical Allele Identifier: PA2830508991

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019731

RCV000084565

RCV003987327

ClinVar Variation:

18103

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Leu630Val	CA127815 NM_201414.3:c.1888C>G