Allele Registry

Canonical Allele Identifier: PA2826270337

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Thr645Met	CA9987104 NM_001204301.2:c.1934C>T