Canonical Allele Identifier: PA916040772
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1931Val
CA16033891
NM_001354896.2:c.5791A>G