Canonical Allele Identifier: PA122088
Gene: UGT1A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 12281
ClinVar RCV Id: RCV000013074 RCV000013073 RCV000147900 RCV000763480 RCV000999563 RCV001810853 RCV004540998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061951.1:p.Tyr487Asp
CA122080
NM_019078.2:c.1459T>G