Canonical Allele Identifier: PA916040598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1784Gly
CA16032911
NM_001354896.2:c.5351A>G