Canonical Allele Identifier: PA193957
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1304Val
CA008754
NM_001127510.3:c.3910A>G