Canonical Allele Identifier: PA2826270918
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Val624Gly
CA127793
NM_001204303.2:c.1871T>G