Canonical Allele Identifier: PA2825641762
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 653217
ClinVar RCV Id: RCV002537302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu1650Gly
CA16032280
NM_001127511.3:c.4949A>G