Canonical Allele Identifier: PA2828009622
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 221112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met1656Thr
CA348841
NM_001354902.2:c.4967T>C