Canonical Allele Identifier: PA2827985370
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met1170Arg
CA008588
NM_001354900.2:c.3509T>G