Canonical Allele Identifier: PA2827996203
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 221112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met1688Thr
CA348841
NM_001354901.2:c.5063T>C