Canonical Allele Identifier: PA2827977727
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717783
ClinVar RCV Id: RCV003743871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly1618Arg
CA16032141
NM_001354899.2:c.4852G>A
CA16032142
NM_001354899.2:c.4852G>C