Allele Registry

Canonical Allele Identifier: PA2825817929

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Ala542Val	CA258118 NM_001136129.3:c.1625C>T