Canonical Allele Identifier: PA2828043969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile1787Val
CA16033891
NM_001354904.2:c.5359A>G