Canonical Allele Identifier: PA2827967118
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met1186Arg
CA008588
NM_001354898.2:c.3557T>G