Canonical Allele Identifier: PA2827995933
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744718
ClinVar RCV Id: RCV002343068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1608Thr
CA16032271
NM_001354901.2:c.4823A>C