Canonical Allele Identifier: PA2826270637
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18098
ClinVar RCV Id: RCV000019725 RCV000020307 RCV000019726 RCV000084563
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Glu656Gly
CA127801
NM_001204302.2:c.1967A>G