Canonical Allele Identifier: PA2827974155
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile516Thr
CA005403
NM_001354899.2:c.1547T>C