Canonical Allele Identifier: PA167922
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1481Ile
CA009548
NM_000038.6:c.4441G>A