Canonical Allele Identifier: PA2827987159
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1712Pro
CA009970
NM_001354900.2:c.5134G>C