Canonical Allele Identifier: PA2827980891
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2583Lys
CA049276
NM_001354899.2:c.7748C>A