Canonical Allele Identifier: PA2827969172
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val1809Ile
CA042161
NM_001354898.2:c.5425G>A