Allele Registry

Canonical Allele Identifier: PA2827947800

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341824.1:p.Ser2581Arg	CA16038140 NM_001354895.2:c.7741A>C CA16038146 NM_001354895.2:c.7743T>A CA16038147 NM_001354895.2:c.7743T>G