Canonical Allele Identifier: PA286681
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu2603Gly
CA014080
NM_001127510.3:c.7808A>G