Canonical Allele Identifier: PA2828048569
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717028
ClinVar RCV Id: RCV003743864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys2464Thr
CA16038207
NM_001354904.2:c.7391A>C