Canonical Allele Identifier: PA2830508982
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 932452
ClinVar RCV Id: RCV001200266

Amino-acid Alleles

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