Canonical Allele Identifier: PA2828033998
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly511Arg
CA16025491
NM_001354904.2:c.1531G>A
CA16025492
NM_001354904.2:c.1531G>C