Canonical Allele Identifier: PA2828047024
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757329
ClinVar RCV Id: RCV002367475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2253Asn
CA16036873
NM_001354904.2:c.6758C>A