Canonical Allele Identifier: PA2828029627
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg2387Lys
CA16038729
NM_001354906.2:c.7160G>A