Allele Registry

Canonical Allele Identifier: PA2825818907

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019728

RCV000084569

ClinVar Variation:

18100

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Thr604Ile	CA127803 NM_001136131.2:c.1811C>T