Canonical Allele Identifier: PA645415134
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 408739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006064.2:p.Asp695Val
CA3983601
NM_006073.4:c.2084A>T