Canonical Allele Identifier: PA2830508787
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Thr695Ala
CA127814
NM_201413.3:c.2083A>G