Allele Registry

Canonical Allele Identifier: PA2830508982

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001200266

ClinVar Variation:

932452

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Leu613Val	CA409806217 NM_201414.3:c.1837T>G