Canonical Allele Identifier: PA2829969147
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 895576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Phe391Leu
CA351074349
NM_021027.3:c.1171T>C
CA351074366
NM_021027.3:c.1173T>A
CA351074371
NM_021027.3:c.1173T>G