Canonical Allele Identifier: PA2828007999
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met1120Arg
CA008588
NM_001354902.2:c.3359T>G