Canonical Allele Identifier: PA113590
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Thr714Ala
CA127814
NM_000484.4:c.2140A>G