Allele Registry

Canonical Allele Identifier: PA2825818002

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001842233

ClinVar Variation:

1342870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Thr588Pro	CA409805542 NM_001136129.3:c.1762A>C