Canonical Allele Identifier: PA2827974412
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly609Arg
CA16025491
NM_001354899.2:c.1825G>A
CA16025492
NM_001354899.2:c.1825G>C