Canonical Allele Identifier: PA658660188
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1834Ile
CA042161
NM_001127510.3:c.5500G>A