Canonical Allele Identifier: PA916039950
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Met909Thr
CA10578343
NM_001354896.2:c.2726T>C