Canonical Allele Identifier: PA645415143
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 287342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006064.2:p.Pro712Leu
CA3983587
NM_006073.4:c.2135C>T