Canonical Allele Identifier: PA156713
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser40Thr
CA023283
NM_001127511.3:c.119G>C