Canonical Allele Identifier: PA2827983490
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr587Ile
CA029849
NM_001354900.2:c.1760C>T