Canonical Allele Identifier: PA2827960035
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val1844Ile
CA042161
NM_001354897.2:c.5530G>A