Canonical Allele Identifier: PA2828035736
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met765Thr
CA10578343
NM_001354904.2:c.2294T>C