Canonical Allele Identifier: PA2580137024
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 2256039
ClinVar RCV Id: RCV004112577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001067.2:p.Cys513Tyr
CA357083009
NM_001076.4:c.1538G>A