Allele Registry

Canonical Allele Identifier: PA2826270871

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Thr570Met	CA9987104 NM_001204303.2:c.1709C>T