Canonical Allele Identifier: PA2827985390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1176Thr
CA008605
NM_001354900.2:c.3527A>C