Canonical Allele Identifier: PA2828052280
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met271Val
CA004131
NM_001354905.2:c.811A>G