Canonical Allele Identifier: PA2827976288
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His1182Tyr
CA008571
NM_001354899.2:c.3544C>T