Canonical Allele Identifier: PA2828037548
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile1038Val
CA16028993
NM_001354904.2:c.3112A>G