Canonical Allele Identifier: PA2828027829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1445798
ClinVar RCV Id: RCV003745443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2119Asp
CA16037019
NM_001354906.2:c.6355A>G