Canonical Allele Identifier: PA2828009281
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1172116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met1547Ile
CA16032097
NM_001354902.2:c.4641G>A
CA16032098
NM_001354902.2:c.4641G>C
CA16032099
NM_001354902.2:c.4641G>T