Canonical Allele Identifier: PA2828040179
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1322Ile
CA16030848
NM_001354904.2:c.3965C>T