Canonical Allele Identifier: PA645459165
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_076980.2:p.Ser181Tyr
CA309374685
NM_024075.5:c.542C>A