Canonical Allele Identifier: PA916040072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1322Val
CA008754
NM_001354896.2:c.3964A>G