Canonical Allele Identifier: PA2827968923
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1732Tyr
CA16032851
NM_001354898.2:c.5195C>A