Canonical Allele Identifier: PA2828016562
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr527Ile
CA029849
NM_001354903.2:c.1580C>T