Allele Registry

Canonical Allele Identifier: PA2825637640

Gene: APC HGNC NCBI

ClinVar Variation Id: 1764696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Ser275Arg	CA16023234 NM_001127511.3:c.823A>C CA16023240 NM_001127511.3:c.825T>A CA16023241 NM_001127511.3:c.825T>G