Canonical Allele Identifier: PA2825450519
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 160119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070914.1:p.Leu112Val
CA272747
NM_001077446.4:c.334C>G