Canonical Allele Identifier: PA916040609
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val1794Ile
CA041569
NM_001354896.2:c.5380G>A