Allele Registry

Canonical Allele Identifier: PA2826270922

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001842233

ClinVar Variation:

1342870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Thr626Pro	CA409805542 NM_001204303.2:c.1876A>C