Allele Registry

Canonical Allele Identifier: PA2827991538

Gene: APC HGNC NCBI

ClinVar Variation Id: 1764696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341830.1:p.Ser234Arg	CA16023234 NM_001354901.2:c.700A>C CA16023240 NM_001354901.2:c.702T>A CA16023241 NM_001354901.2:c.702T>G