Canonical Allele Identifier: PA2828005096
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1057Thr
CA008605
NM_001354905.2:c.3170A>C