Canonical Allele Identifier: PA286679
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu2585Gly
CA014080
NM_001127511.3:c.7754A>G