Canonical Allele Identifier: PA2828052455
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala289Val
CA16024253
NM_001354905.2:c.866C>T