Canonical Allele Identifier: PA645415138
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 408741
ClinVar RCV Id: RCV003638668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006064.2:p.Asn698Asp
CA16612100
NM_006073.4:c.2092A>G