Allele Registry

Canonical Allele Identifier: PA2828960773

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Thr607Met	CA9987104 NM_001385253.1:c.1820C>T