Canonical Allele Identifier: PA2828005945
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala1198Val
CA008903
NM_001354905.2:c.3593C>T