Canonical Allele Identifier: PA122064
Gene: UGT1A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 12272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995584.1:p.Gly40Glu
CA122054
NM_205862.3:c.119G>A