Canonical Allele Identifier: PA2827978081
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1725Pro
CA009970
NM_001354899.2:c.5173G>C