Canonical Allele Identifier: PA2828053838
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr468Ile
CA029849
NM_001354905.2:c.1403C>T