Canonical Allele Identifier: PA2825021881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1834Ile
CA042161
NM_000038.6:c.5500G>A