Canonical Allele Identifier: PA2825817995
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Val586Gly
CA127793
NM_001136129.3:c.1757T>G