Allele Registry

Canonical Allele Identifier: PA122110

Gene: UGT1A9 HGNC NCBI

ClinVar Allele:

27325

ClinVar RCV:

RCV000013079

RCV000013080

RCV004528106

ClinVar Variation:

12286

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Asn397Asp	CA122104 NM_021027.3:c.1189A>G