Canonical Allele Identifier: PA916040949
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2089Met
CA10578423
NM_001354896.2:c.6267A>G