Canonical Allele Identifier: PA2827947938
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2626Ile
CA014137
NM_001354895.2:c.7877C>T