Canonical Allele Identifier: PA2826270638
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18087
ClinVar RCV Id: RCV000019713 RCV001386879 RCV002272024
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Glu656Gln
CA127790
NM_001204302.2:c.1966G>C