Canonical Allele Identifier: PA2827959751
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 221112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met1757Thr
CA348841
NM_001354897.2:c.5270T>C