Canonical Allele Identifier: PA2828020667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile1203Val
CA008754
NM_001354903.2:c.3607A>G