Canonical Allele Identifier: PA2827950142
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1777096
ClinVar RCV Id: RCV002403589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu566Ser
CA16024897
NM_001354896.2:c.1697T>C