Canonical Allele Identifier: PA2827975613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 921338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp988Asn
CA16028000
NM_001354899.2:c.2962G>A