Canonical Allele Identifier: PA2827980387
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 658256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2431Cys
CA16037401
NM_001354899.2:c.7292C>G