Canonical Allele Identifier: PA193956
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile1304Val
CA008754
NM_000038.6:c.3910A>G