Canonical Allele Identifier: PA916039599
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser570Cys
CA16024927
NM_001354896.2:c.1709C>G