Canonical Allele Identifier: PA2827968721
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala1675Thr
CA16032477
NM_001354898.2:c.5023G>A