Canonical Allele Identifier: PA2829896331
Gene: UGT1A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1703141
ClinVar RCV Id: RCV002280264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061950.2:p.Trp351Gly
CA351073312
NM_019077.3:c.1051T>G