Canonical Allele Identifier: PA916039597
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 656514
ClinVar RCV Id: RCV003653381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu566Met
CA16024894
NM_001354896.2:c.1696T>A