Canonical Allele Identifier: PA122085
Gene: UGT1A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12281
ClinVar RCV Id: RCV000013074 RCV000013073 RCV000147900 RCV000763480 RCV000999563 RCV001810853 RCV004540998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061950.2:p.Tyr483Asp
CA122080
NM_019077.3:c.1447T>G