Canonical Allele Identifier: PA122014
Gene: UGT1A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 12267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001063.2:p.Ser374Phe
CA122007
NM_001072.4:c.1121C>T