Canonical Allele Identifier: PA2827980492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2462Asn
CA013697
NM_001354899.2:c.7384G>A