Canonical Allele Identifier: PA348844
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 221112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met1747Thr
CA348841
NM_001127510.3:c.5240T>C