Canonical Allele Identifier: PA2825817905
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Glu534Asp
CA127797
NM_001136129.3:c.1602G>C
CA409806514
NM_001136129.3:c.1602G>T