Canonical Allele Identifier: PA916041465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2514Arg
CA16037616
NM_001354896.2:c.7541A>G