Canonical Allele Identifier: PA2825817979
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Thr583Ala
CA127814
NM_001136129.3:c.1747A>G