Canonical Allele Identifier: PA173829
Gene: UGT1A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 160230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001063.2:p.Val410Leu
CA173822
NM_001072.4:c.1228G>T
CA351074993
NM_001072.4:c.1228G>C