Canonical Allele Identifier: PA2827978136
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly1739Asp
CA16032918
NM_001354899.2:c.5216G>A