Canonical Allele Identifier: PA916041608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2644Ile
CA014137
NM_001354896.2:c.7931C>T