Canonical Allele Identifier: PA2828029073
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717028
ClinVar RCV Id: RCV003743864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys2307Thr
CA16038207
NM_001354906.2:c.6920A>C