Canonical Allele Identifier: PA2827974329
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val581Ile
CA006055
NM_001354899.2:c.1741G>A