Canonical Allele Identifier: PA2829896427
Gene: UGT1A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 218786
ClinVar RCV Id: RCV000203111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061950.2:p.Ala474Ser
CA249315
NM_019077.3:c.1420G>T