Canonical Allele Identifier: PA2827987426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val1793Ile
CA042161
NM_001354900.2:c.5377G>A