Canonical Allele Identifier: PA2828043817
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.His1771Pro
CA010592
NM_001354904.2:c.5312A>C