Canonical Allele Identifier: PA2827979001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2008Asn
CA16034696
NM_001354899.2:c.6022G>A