Canonical Allele Identifier: PA2825818390
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Glu609Asp
CA127797
NM_001136130.2:c.1827G>C
CA409806514
NM_001136130.2:c.1827G>T