Canonical Allele Identifier: PA2827992591
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 83212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile579Val
CA006325
NM_001354901.2:c.1735A>G