Allele Registry

Canonical Allele Identifier: PA2827499065

Gene: UGT2B7 HGNC NCBI

ClinVar RCV:

RCV001028136

ClinVar Variation:

828226

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336497.1:p.Tyr19His	CA2944699 NM_001349568.2:c.55T>C CA98844870 NM_001349568.2:c.54_55delinsTC