Canonical Allele Identifier: PA2827968928
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1732Cys
CA16032852
NM_001354898.2:c.5195C>G