Canonical Allele Identifier: PA2827947126
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2379Pro
CA16036870
NM_001354895.2:c.7135A>C