Canonical Allele Identifier: PA916041530
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2569Leu
CA16037955
NM_001354896.2:c.7706A>T