Canonical Allele Identifier: PA2827998841
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2493Cys
CA16037960
NM_001354901.2:c.7477A>T