Canonical Allele Identifier: PA297881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile2224Val
CA012361
NM_000038.6:c.6670A>G