Allele Registry

Canonical Allele Identifier: PA2829969114

Gene: UGT1A9 HGNC NCBI

ClinVar Variation Id: 288098

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Arg364Cys	CA2180010 NM_021027.3:c.1090C>T