Canonical Allele Identifier: PA2826270913
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18096
ClinVar Variation Id: 1457308
ClinVar RCV Id: RCV001947096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Ile623Val
CA127799
NM_001204303.2:c.1867A>G
CA2573157339
NM_001204303.2:c.1866_1867delinsTG