Canonical Allele Identifier: PA156727
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1217Thr
CA008605
NM_000038.6:c.3650A>C