Allele Registry

Canonical Allele Identifier: PA2826270658

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084574

RCV003509495

ClinVar Variation:

98240

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Ile679Thr	CA225511 NM_001204302.2:c.2036T>C