Canonical Allele Identifier: PA2828053914
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly477Arg
CA16025491
NM_001354905.2:c.1429G>A
CA16025492
NM_001354905.2:c.1429G>C