Canonical Allele Identifier: PA2827974389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr600Ile
CA029849
NM_001354899.2:c.1799C>T