Allele Registry

Canonical Allele Identifier: PA2825817993

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084574

RCV003509495

ClinVar Variation:

98240

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Ile585Thr	CA225511 NM_001136129.3:c.1754T>C