Canonical Allele Identifier: PA2828043411
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly1710Arg
CA042181
NM_001354904.2:c.5128G>A
CA16033377
NM_001354904.2:c.5128G>C