Canonical Allele Identifier: PA272749
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 160119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076980.2:p.Leu112Val
CA272747
NM_024075.5:c.334C>G