Canonical Allele Identifier: PA2828013406
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Arg2510Lys
CA16038729
NM_001354905.2:c.7529G>A