Allele Registry

Canonical Allele Identifier: PA916028587

Gene: UGT2B7 HGNC NCBI

ClinVar Allele:

816557

ClinVar RCV:

RCV001028970

ClinVar Variation:

829053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317648.1:p.Ala71Ser	CA2944536 NM_001330719.2:c.211G>T