Canonical Allele Identifier: PA096598
Gene: TSEN34 HGNC NCBI
ClinVar Allele:
17163
ClinVar RCV:
RCV000002206
ClinVar Variation:
2124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070914.1:p.Arg58Trp
CA339948
NM_001077446.4:c.172C>T