Canonical Allele Identifier: PA2828054887
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met731Thr
CA10578343
NM_001354905.2:c.2192T>C