Canonical Allele Identifier: PA2741827719
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 2619425
ClinVar RCV Id: RCV004363206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001067.2:p.Ala503Thr
CA2942369
NM_001076.4:c.1507G>A