Allele Registry

Canonical Allele Identifier: PA2829969159

Gene: UGT1A9 HGNC NCBI

ClinVar RCV:

RCV000729304

ClinVar Variation:

594091

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Asn397His	CA67596366 NM_021027.3:c.1189A>C