Allele Registry

Canonical Allele Identifier: PA2826270613

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Thr626Met	CA9987104 NM_001204302.2:c.1877C>T