Allele Registry

Canonical Allele Identifier: PA2830508962

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Thr588Met	CA9987104 NM_201414.3:c.1763C>T