Allele Registry

Canonical Allele Identifier: PA2827997280

Gene: APC HGNC NCBI

ClinVar Variation Id: 489476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341830.1:p.Asp2020Ala	CA044147 NM_001354901.2:c.6059A>C