Canonical Allele Identifier: PA645402307
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2598Asn
CA049224
NM_001127510.3:c.7793C>A