Canonical Allele Identifier: PA2827945063
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 221112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Met1747Thr
CA348841
NM_001354895.2:c.5240T>C