Canonical Allele Identifier: PA2828019806
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg863Cys
CA035367
NM_001354906.2:c.2587C>T