Canonical Allele Identifier: PA2828019558
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730350
ClinVar RCV Id: RCV002326526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr829Lys
CA16028645
NM_001354906.2:c.2486C>A