Allele Registry

Canonical Allele Identifier: PA2825817903

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Thr532Met	CA9987104 NM_001136129.3:c.1595C>T