Canonical Allele Identifier: PA2828024881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.His1682Pro
CA043314
NM_001354906.2:c.5045A>C