Allele Registry

Canonical Allele Identifier: PA916028602

Gene: UGT2B7 HGNC NCBI

ClinVar RCV:

RCV001028136

ClinVar Variation:

828226

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317648.1:p.Tyr268His	CA2944699 NM_001330719.2:c.802T>C CA98844870 NM_001330719.2:c.801_802delinsTC