Canonical Allele Identifier: PA2827971729
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile2590Thr
CA16038374
NM_001354898.2:c.7769T>C