Canonical Allele Identifier: PA2828055323
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp862Gly
CA16028046
NM_001354905.2:c.2585A>G