Allele Registry

Canonical Allele Identifier: PA2825818389

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Thr607Met	CA9987104 NM_001136130.2:c.1820C>T