Allele Registry

Canonical Allele Identifier: PA2827989874

Gene: APC HGNC NCBI

ClinVar Variation Id: 2586969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341829.1:p.Ser2540Arg	CA16038140 NM_001354900.2:c.7618A>C CA16038146 NM_001354900.2:c.7620T>A CA16038147 NM_001354900.2:c.7620T>G