Canonical Allele Identifier: PA2829969141
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709801
ClinVar RCV Id: RCV002290143
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Met388Ile
CA2180023
NM_021027.3:c.1164G>A
CA351074294
NM_021027.3:c.1164G>C
CA351074295
NM_021027.3:c.1164G>T