Canonical Allele Identifier: PA2827991406
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His196Arg
CA048853
NM_001354901.2:c.587A>G