Canonical Allele Identifier: PA916040583
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1771Pro
CA009970
NM_001354896.2:c.5311G>C