Canonical Allele Identifier: PA2825433286
Gene: UBTF HGNC NCBI

Linked Data

ClinVar Variation Id: 437909
ClinVar RCV Id: RCV000504592 RCV000505522 RCV000625527 RCV000845031 RCV001265907 RCV001195293 RCV001566123 RCV001420236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070151.1:p.Glu210Lys
CA399765298
NM_001076683.2:c.628G>A