Canonical Allele Identifier: PA2827957980
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met1221Arg
CA008588
NM_001354897.2:c.3662T>G