Canonical Allele Identifier: PA2827942954
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gly1116Asp
CA008298
NM_001354895.2:c.3347G>A