Canonical Allele Identifier: PA2825818449
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Glu637Gly
CA127801
NM_001136130.2:c.1910A>G