Canonical Allele Identifier: PA2828022818
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1172116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Met1355Ile
CA16032097
NM_001354906.2:c.4065G>A
CA16032098
NM_001354906.2:c.4065G>C
CA16032099
NM_001354906.2:c.4065G>T