Canonical Allele Identifier: PA2830508778
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 1912162
ClinVar RCV Id: RCV002578767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Ile683Met
CA409805627
NM_201413.3:c.2049C>G