Canonical Allele Identifier: PA2829895900
Gene: UGT1A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709802
ClinVar RCV Id: RCV002290144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061948.1:p.Arg400Leu
CA351074944
NM_019075.4:c.1199G>T