Allele Registry

Canonical Allele Identifier: PA122095

Gene: UGT1A7 HGNC NCBI

ClinVar RCV:

RCV000013076

RCV003488338

RCV003987318

ClinVar Variation:

12283

HGVS (amino-acid)	Matching Registered Transcripts
NP_061950.2:p.Gln354Arg	CA122091 NM_019077.3:c.1061A>G