Canonical Allele Identifier: PA2827996185
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 801036
ClinVar RCV Id: RCV000985308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Phe1682Cys
CA16032748
NM_001354901.2:c.5045T>G