Canonical Allele Identifier: PA166143
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2759His
CA014525
NM_001127510.3:c.8276G>A