Canonical Allele Identifier: PA2829124942
Gene: TSEN34 HGNC NCBI

Linked Data

ClinVar Variation Id: 212446
ClinVar RCV Id: RCV000193230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373669.1:p.Gln90Glu
CA206570
NM_001386740.1:c.268C>G