Canonical Allele Identifier: PA2827986805
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717783
ClinVar RCV Id: RCV003743871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1605Arg
CA16032141
NM_001354900.2:c.4813G>A
CA16032142
NM_001354900.2:c.4813G>C