Allele Registry

Canonical Allele Identifier: PA2825817992

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003223103

ClinVar Variation:

2498894

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Ile585Phe	CA409805555 NM_001136129.3:c.1753A>T