Allele Registry

Canonical Allele Identifier: PA2825399052

Gene: UGT2B7 HGNC NCBI

ClinVar RCV:

RCV000891815

RCV001028973

ClinVar Variation:

718812

HGVS (amino-acid)	Matching Registered Transcripts
NP_001065.2:p.Leu46Pro	CA2944517 NM_001074.4:c.137T>C