Canonical Allele Identifier: PA2828047021
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2253Pro
CA16036870
NM_001354904.2:c.6757A>C