Canonical Allele Identifier: PA2827968889
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 221112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met1722Thr
CA348841
NM_001354898.2:c.5165T>C