Canonical Allele Identifier: PA206572
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 212446
ClinVar RCV Id: RCV000193230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076980.2:p.Gln90Glu
CA206570
NM_024075.5:c.268C>G