Canonical Allele Identifier: PA2828960841
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.Thr658Ala
CA127814
NM_001385253.1:c.1972A>G