Canonical Allele Identifier: PA2827992352
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser493Cys
CA16024927
NM_001354901.2:c.1478C>G