Canonical Allele Identifier: PA916039680
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly655Arg
CA16025491
NM_001354896.2:c.1963G>A
CA16025492
NM_001354896.2:c.1963G>C