Allele Registry

Canonical Allele Identifier: PA2826270891

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Leu595Val	CA409806217 NM_001204303.2:c.1783T>G