Canonical Allele Identifier: PA2826641857
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 160119
ClinVar RCV Id: RCV000147762 RCV002055938 RCV001136205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269261.1:p.Leu112Val
CA272747
NM_001282332.2:c.334C>G