Canonical Allele Identifier: PA2827955880
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566964
ClinVar RCV Id: RCV003306834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser562Pro
CA16024924
NM_001354897.2:c.1684T>C