Allele Registry

Canonical Allele Identifier: PA2829896070

Gene: UGT1A8 HGNC NCBI

ClinVar Variation Id: 288098

HGVS (amino-acid)	Matching Registered Transcripts
NP_061949.3:p.Arg364Cys	CA2180010 NM_019076.5:c.1090C>T