Canonical Allele Identifier: PA2830508776
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Glu674Gly
CA127801
NM_201413.3:c.2021A>G