Canonical Allele Identifier: PA2825644614
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717028
ClinVar RCV Id: RCV003743864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys2572Thr
CA16038207
NM_001127511.3:c.7715A>C