Canonical Allele Identifier: PA2827977921
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 574199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1679Pro
CA16032519
NM_001354899.2:c.5035T>C