Canonical Allele Identifier: PA2828055338
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Tyr867Asp
CA16028076
NM_001354905.2:c.2599T>G