Canonical Allele Identifier: PA2830508999
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958817.1:p.Thr639Ala
CA127814
NM_201414.3:c.1915A>G