Canonical Allele Identifier: PA2827966374
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp964Gly
CA034127
NM_001354898.2:c.2891A>G