Canonical Allele Identifier: PA297773
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Val803Ile
CA007489
NM_001127511.3:c.2407G>A