Canonical Allele Identifier: PA2827968959
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1742Asp
CA16032918
NM_001354898.2:c.5225G>A