Canonical Allele Identifier: PA2828016170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser451Cys
CA16024927
NM_001354903.2:c.1352C>G