Allele Registry

Canonical Allele Identifier: PA2825818842

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Thr553Met	CA9987104 NM_001136131.2:c.1658C>T