Canonical Allele Identifier: PA2828004143
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp2428Gly
CA16037756
NM_001354902.2:c.7283A>G