Canonical Allele Identifier: PA2827980595
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2491Gly
CA16037756
NM_001354899.2:c.7472A>G