Canonical Allele Identifier: PA2826641881
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 290843
ClinVar RCV Id: RCV000311301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269261.1:p.Ser181Tyr
CA309374685
NM_001282332.2:c.542C>A