Canonical Allele Identifier: PA156726
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1199Thr
CA008605
NM_001127511.3:c.3596A>C