Canonical Allele Identifier: PA2828049102
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg2544Lys
CA16038729
NM_001354904.2:c.7631G>A