Canonical Allele Identifier: PA2825024812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717028
ClinVar RCV Id: RCV003743864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys2590Thr
CA16038207
NM_000038.6:c.7769A>C