Allele Registry

Canonical Allele Identifier: PA2830508750

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Thr644Met	CA9987104 NM_201413.3:c.1931C>T