Canonical Allele Identifier: PA112140
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Ser375Phe
CA122007
NM_000463.3:c.1124C>T