Allele Registry

Canonical Allele Identifier: PA2827955237

Gene: APC HGNC NCBI

ClinVar Variation Id: 1764696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341826.1:p.Ser303Arg	CA16023234 NM_001354897.2:c.907A>C CA16023240 NM_001354897.2:c.909T>A CA16023241 NM_001354897.2:c.909T>G