Allele Registry

Canonical Allele Identifier: PA122009

Gene: UGT1A6 HGNC NCBI

ClinVar RCV:

RCV000013054

RCV001851815

RCV003387719

ClinVar Variation:

12267

HGVS (amino-acid)	Matching Registered Transcripts
NP_995584.1:p.Ser107Phe	CA122007 NM_205862.3:c.320C>T