Canonical Allele Identifier: PA111994
Gene: UGT1A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 12267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009051.1:p.Ser376Phe
CA122007
NM_007120.3:c.1127C>T