Canonical Allele Identifier: PA2826641928
Gene: TSEN34 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269262.2:p.Arg58Trp
CA339948
NM_001282333.2:c.172C>T