Allele Registry

Canonical Allele Identifier: PA2825818926

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084574

RCV003509495

ClinVar Variation:

98240

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Ile606Thr	CA225511 NM_001136131.2:c.1817T>C