Canonical Allele Identifier: PA2828029122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2841673
ClinVar RCV Id: RCV003652405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly2314Arg
CA16038249
NM_001354906.2:c.6940G>A
CA16038250
NM_001354906.2:c.6940G>C