Allele Registry

Canonical Allele Identifier: PA122013

Gene: UGT1A9 HGNC NCBI

ClinVar Variation Id: 12267

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Ser372Phe	CA122007 NM_021027.3:c.1115C>T