Canonical Allele Identifier: PA2827976772
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1330Val
CA008903
NM_001354899.2:c.3989C>T