Canonical Allele Identifier: PA2827947638
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1321396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2533Cys
CA16037837
NM_001354895.2:c.7598C>G