Canonical Allele Identifier: PA214608
Gene: UBE2T HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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