Canonical Allele Identifier: PA2828008572
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His1737Pro
CA010592
NM_001354905.2:c.5210A>C