Allele Registry

Canonical Allele Identifier: PA2827962487

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341826.1:p.Ser2591Arg	CA16038140 NM_001354897.2:c.7771A>C CA16038146 NM_001354897.2:c.7773T>A CA16038147 NM_001354897.2:c.7773T>G