Canonical Allele Identifier: PA2826641920
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 426378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269262.2:p.Thr32Pro
CA309372747
NM_001282333.2:c.94A>C