Canonical Allele Identifier: PA2827977796
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1643Thr
CA16032296
NM_001354899.2:c.4927G>A