Canonical Allele Identifier: PA916041837
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2834Gln
CA050856
NM_001354896.2:c.8501G>A