Canonical Allele Identifier: PA2827947853
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2598Asn
CA049224
NM_001354895.2:c.7793C>A