Canonical Allele Identifier: PA2825399239
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 3186192
ClinVar RCV Id: RCV004479590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001067.2:p.Ser15Gly
CA98760679
NM_001076.4:c.43A>G