Allele Registry

Canonical Allele Identifier: PA2825818895

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019731

RCV000084565

RCV003987327

ClinVar Variation:

18103

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Leu595Val	CA127815 NM_001136131.2:c.1783C>G