Canonical Allele Identifier: PA645415141
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 240286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006064.2:p.Arg711Cys
CA3983590
NM_006073.4:c.2131C>T