Canonical Allele Identifier: PA2826270909
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Thr621Ala
CA127814
NM_001204303.2:c.1861A>G