Allele Registry

Canonical Allele Identifier: PA2827988215

Gene: APC HGNC NCBI

ClinVar Variation Id: 489476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341829.1:p.Asp2038Ala	CA044147 NM_001354900.2:c.6113A>C