Canonical Allele Identifier: PA2827977908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly1675Arg
CA16032494
NM_001354899.2:c.5023G>A
CA16032495
NM_001354899.2:c.5023G>C