Canonical Allele Identifier: PA2827989673
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp2478Gly
CA16037756
NM_001354900.2:c.7433A>G