Canonical Allele Identifier: PA214608
Gene: UBE2T HGNC NCBI

Linked Data

ClinVar Variation Id: 199436
ClinVar RCV Id: RCV000180789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054895.1:p.Gln2Glu
CA214607
NM_014176.4:c.4C>G