Canonical Allele Identifier: PA2825643962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757329
ClinVar RCV Id: RCV002367475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2361Asn
CA16036873
NM_001127511.3:c.7082C>A