Canonical Allele Identifier: PA173828
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 160230
ClinVar RCV Id: RCV000147894 RCV000731958 RCV004532662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Val408Leu
CA173822
NM_021027.3:c.1222G>T
CA351074993
NM_021027.3:c.1222G>C