Canonical Allele Identifier: PA916042679
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn934Thr
CA008605
NM_001354906.2:c.2801A>C