Canonical Allele Identifier: PA2829895892
Gene: UGT1A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709801
ClinVar RCV Id: RCV002290143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061948.1:p.Met388Ile
CA2180023
NM_019075.4:c.1164G>A
CA351074294
NM_019075.4:c.1164G>C
CA351074295
NM_019075.4:c.1164G>T