Allele Registry

Canonical Allele Identifier: PA122012

Gene: UGT1A7 HGNC NCBI

ClinVar RCV:

RCV000013054

RCV001851815

RCV003387719

ClinVar Variation:

12267

HGVS (amino-acid)	Matching Registered Transcripts
NP_061950.2:p.Ser372Phe	CA122007 NM_019077.3:c.1115C>T