Canonical Allele Identifier: PA2827971677
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2841673
ClinVar RCV Id: RCV003652405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly2572Arg
CA16038249
NM_001354898.2:c.7714G>A
CA16038250
NM_001354898.2:c.7714G>C