Canonical Allele Identifier: PA2827941188
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser552Cys
CA16024927
NM_001354895.2:c.1655C>G