Canonical Allele Identifier: PA2825818844
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129603.1:p.Glu555Asp
CA127797
NM_001136131.2:c.1665G>C
CA409806514
NM_001136131.2:c.1665G>T