Canonical Allele Identifier: PA2827977074
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1420Ile
CA16030848
NM_001354899.2:c.4259C>T