Canonical Allele Identifier: PA2827947494
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp2490Asn
CA013697
NM_001354895.2:c.7468G>A