Canonical Allele Identifier: PA2827975949
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val1087Met
CA035105
NM_001354899.2:c.3259G>A