Canonical Allele Identifier: PA2828020233
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1116Thr
CA008605
NM_001354903.2:c.3347A>C