Canonical Allele Identifier: PA2580478686
Gene: UTP23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2307698
ClinVar RCV Id: RCV004151553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115710.2:p.Ala214Ser
CA4852623
NM_032334.3:c.640G>T