Canonical Allele Identifier: PA2827999465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2679Thr
CA336116
NM_001354901.2:c.8036T>C