Canonical Allele Identifier: PA2829969161
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 502603
ClinVar RCV Id: RCV000593141
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Arg400His
CA2180031
NM_021027.3:c.1199G>A