Canonical Allele Identifier: PA2828012479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp2359Gly
CA16037756
NM_001354905.2:c.7076A>G