Canonical Allele Identifier: PA2828016000
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser269Cys
CA16024927
NM_001354906.2:c.806C>G