Canonical Allele Identifier: PA2829124974
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 290843
ClinVar RCV Id: RCV000311301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373669.1:p.Ser181Tyr
CA309374685
NM_001386740.1:c.542C>A