Allele Registry

Canonical Allele Identifier: PA2826270633

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Leu651Val	CA409806217 NM_001204302.2:c.1951T>G