Canonical Allele Identifier: PA2827943598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ile1304Val
CA008754
NM_001354895.2:c.3910A>G