Canonical Allele Identifier: PA645459156
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 426378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076980.2:p.Thr32Pro
CA309372747
NM_024075.5:c.94A>C