Canonical Allele Identifier: PA2828013049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile2455Thr
CA16038374
NM_001354905.2:c.7364T>C