Canonical Allele Identifier: PA2825635205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760169
ClinVar RCV Id: RCV002400545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2566Ile
CA16038051
NM_001127510.3:c.7697G>T