Canonical Allele Identifier: PA2827978051
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746238
ClinVar RCV Id: RCV002344319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1716Thr
CA16032764
NM_001354899.2:c.5147A>C