Canonical Allele Identifier: PA645415147
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 408735
ClinVar RCV Id: RCV002429506 RCV002525570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006064.2:p.Ser715Gly
CA3983584
NM_006073.4:c.2143A>G