Allele Registry

Canonical Allele Identifier: PA2829896087

Gene: UGT1A8 HGNC NCBI

ClinVar RCV:

RCV000729304

ClinVar Variation:

594091

HGVS (amino-acid)	Matching Registered Transcripts
NP_061949.3:p.Asn397His	CA67596366 NM_019076.5:c.1189A>C