Canonical Allele Identifier: PA2825635048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 658256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2459Cys
CA16037401
NM_001127510.3:c.7376C>G