Canonical Allele Identifier: PA2827998990
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2841673
ClinVar RCV Id: RCV003652405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly2538Arg
CA16038249
NM_001354901.2:c.7612G>A
CA16038250
NM_001354901.2:c.7612G>C