Canonical Allele Identifier: PA916042044
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133505
ClinVar Variation Id: 1056172
ClinVar RCV Id: RCV002242581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser26Arg
CA025425
NM_001354902.2:c.78C>A
CA360611868
NM_001354902.2:c.76A>C
CA360611883
NM_001354902.2:c.78C>G