Canonical Allele Identifier: PA915954934
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 791440
ClinVar RCV Id: RCV000974405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001067.2:p.Lys527Arg
CA2942354
NM_001076.4:c.1580A>G