Canonical Allele Identifier: PA2829896356
Gene: UGT1A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 498022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061950.2:p.Val383Ile
CA2180020
NM_019077.3:c.1147G>A