Canonical Allele Identifier: PA2828029338
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2510Ile
CA014100
NM_001354903.2:c.7529C>T