Canonical Allele Identifier: PA173831
Gene: UGT1A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 160230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009051.1:p.Val412Leu
CA173822
NM_007120.3:c.1234G>T
CA351074993
NM_007120.3:c.1234G>C