Canonical Allele Identifier: PA2827986781
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1172116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met1597Ile
CA16032097
NM_001354900.2:c.4791G>A
CA16032098
NM_001354900.2:c.4791G>C
CA16032099
NM_001354900.2:c.4791G>T