Canonical Allele Identifier: PA2827976310
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1189Thr
CA008605
NM_001354899.2:c.3566A>C