Canonical Allele Identifier: PA2827980911
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1064027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2590Ile
CA16038397
NM_001354899.2:c.7769A>T