Canonical Allele Identifier: PA2827955879
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser562Cys
CA16024927
NM_001354897.2:c.1685C>G