Allele Registry

Canonical Allele Identifier: PA2828960849

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084574

RCV003509495

ClinVar Variation:

98240

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Ile660Thr	CA225511 NM_001385253.1:c.1979T>C