Canonical Allele Identifier: PA2825399241
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 3186197
ClinVar RCV Id: RCV004479595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001067.2:p.Ser19Arg
CA2942783
NM_001076.4:c.57C>A
CA357087801
NM_001076.4:c.57C>G
CA357087812
NM_001076.4:c.55A>C