Canonical Allele Identifier: PA2828048731
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile2489Thr
CA16038374
NM_001354904.2:c.7466T>C