Canonical Allele Identifier: PA2827992627
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg594Gly
CA16025594
NM_001354901.2:c.1780A>G