Canonical Allele Identifier: PA2826990768
Gene: UTP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305320.1:p.Arg482Trp
CA116052
NM_001318391.2:c.1444C>T