Canonical Allele Identifier: PA2827969830
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp2011Asn
CA16034696
NM_001354898.2:c.6031G>A