Canonical Allele Identifier: PA2829124923
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 426378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373669.1:p.Thr32Pro
CA309372747
NM_001386740.1:c.94A>C